NDC Product
Human Otc DrugMenthol Cough Drops Creamy Strawberry Flavor NDC 10202-012
- Generic Name
- Menthol And Pectin
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Substance Identification & Data
This profile provides standardized clinical and technical data for Soybean Lecithin, uniquely identified by the FDA Unique Ingredient Identifier (UNII) 1DI56QDM62.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 8030-76-0 and the RxNorm Concept ID (RxCUI) 579598. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
Detailed Substance Profile
Preferred Name
SOYBEAN LECITHIN
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
1DI56QDM62
The specific atomic composition represented as a molecular structure string.
NCI Thesaurus
National Cancer Institute reference terminology for clinical and research data.
Substance Type
structurallyDiverse
ISO 11238 classification category (e.g., Chemical, Polymer, Protein).
ITIS TSN
26716
Taxonomic Serial Number for species identified in the Integrated Taxonomic Information System.
NCBI Taxonomy
3847
Unique numeric identifier used to specify biological species in the NCBI database.
USDA PLANTS ID
GLMA4
Botanical identifier maintained by the U.S. Department of Agriculture.
GRIN Nomen ID
17711
Identifier from the Germplasm Resources Information Network botanical database.
MPNS Record
WCS-2827366
Record ID from the Kew Royal Botanic Gardens Medicinal Plants Name Service.
Synonyms and Nomenclature
This section provides a complete list of nomenclature and identifier mappings for Soybean Lecithin. Identifiers are organized into official regulatory terms, commercial trade names, and technical systematic synonyms used to ensure accurate identification across clinical pharmaceutical databases, regulatory filings, and electronic health records.
Common Names & Synonyms
LECITHIN, SOY
CN
LECITHIN, SOYBEAN
CN
LECITHIN, SOYBEAN [II]
CN
PHOSPHOLIPIDS SOYBEAN [WHO-DD]
CN
SOY LECITHIN
CN
SOY LECITHIN [VANDF]
CN
SOY LECITHINS
CN
SOY PHOSPHATIDES
CN
SOY PHOSPHOLIPIDS
CN
SOYA LECITHIN
CN
SOYA LECITHINS
CN
SOYA PHOSPHOLIPIDS
CN
SOYBEAN LECITHIN
CN
SOYBEAN LECITHINS
CN
SOYBEAN PHOSPHOLIPIDS
CN
Brand / Trade Names
ALCOLEC BS
BN
ALCOLEC GRANULES
BN
ALCOLEC S
BN
LIPOID P 20
BN
LIPOID P 45
BN
LIPOID P 75
BN
LIPOID S 20
BN
LIPOID S 45
BN
LIPOID S 75
BN
Systematic Nomenclature
GLYCINE MAX PHOSPHOLIPIDS
SYS
Technical Codes
E-322(I)
CD
INS NO.322(I)
CD
INS-322(I)
CD
NDC Products Containing SOYBEAN LECITHIN
This unique ingredient identifier is listed as an ingredient or substance in the following products in the NDC directory:
Manufacturer Quick Index
Note: Due to the high number of listings (500), only Active Listings are currently displayed. Display is limited to the first 200 products.
Showing 200 active products
7-ELEVEN
Active Listing
NDC Product
Human Otc DrugMenthol Cough Drops Honey Vanilla Flavor NDC 10202-013
- Generic Name
- Menthol
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
ALMAY
NDC Product
Human Otc DrugAlmay Clear Complexion Makeup Foundation True Beige NDC 0311-0754
- Generic Name
- Salicylic Acid
- Dosage Form
- Emulsion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAlmay Clear Complexion Makeup Foundation Sun Beige NDC 0311-0755
- Generic Name
- Salicylic Acid
- Dosage Form
- Emulsion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAlmay Clear Complexion Makeup Foundation Porcelain NDC 0311-0756
- Generic Name
- Salicylic Acid
- Dosage Form
- Emulsion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAlmay Clear Complexion Makeup Foundation Ivory NDC 0311-0757
- Generic Name
- Salicylic Acid
- Dosage Form
- Emulsion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAlmay Clear Complexion Makeup Foundation Buff NDC 0311-0758
- Generic Name
- Salicylic Acid
- Dosage Form
- Emulsion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAlmay Clear Complexion Makeup Foundation Naked NDC 0311-0759
- Generic Name
- Salicylic Acid
- Dosage Form
- Emulsion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAlmay Clear Complexion Makeup Foundation Neutral NDC 0311-0760
- Generic Name
- Salicylic Acid
- Dosage Form
- Emulsion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAlmay Clear Complexion Makeup Foundation Fresh Beige NDC 0311-0761
- Generic Name
- Salicylic Acid
- Dosage Form
- Emulsion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAlmay Clear Complexion Makeup Foundation Golden Caramel NDC 0311-0762
- Generic Name
- Salicylic Acid
- Dosage Form
- Emulsion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAlmay Clear Complexion Makeup Foundation Golden NDC 0311-0763
- Generic Name
- Salicylic Acid
- Dosage Form
- Emulsion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAlmay Clear Complexion Makeup Foundation Caramel NDC 0311-0764
- Generic Name
- Salicylic Acid
- Dosage Form
- Emulsion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAlmay Clear Complexion Makeup Foundation Rich Cocoa NDC 0311-0765
- Generic Name
- Salicylic Acid
- Dosage Form
- Emulsion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAlmay Clear Complexion Makeup Foundation Mahogany NDC 0311-0766
- Generic Name
- Salicylic Acid
- Dosage Form
- Emulsion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAlmay Clear Complexion Makeup Foundation Mocha NDC 0311-0767
- Generic Name
- Salicylic Acid
- Dosage Form
- Emulsion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAlmay Clear Complexion Makeup Foundation Natural Tan NDC 0311-0782
- Generic Name
- Salicylic Acid
- Dosage Form
- Emulsion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Actavis Pharma, Inc.
NDC Product
Human Prescription DrugAzelaic Acid NDC 0591-2131
- Generic Name
- Azelaic Acid
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmbrisentan NDC 0591-2405
- Generic Name
- Ambrisentan
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Ambrisentan
- Dosage Form
- Tablet, Film Coated
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Ambrisentan
- Dosage Form
- Tablet, Film Coated
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugAmbrisentan NDC 0591-2406
- Generic Name
- Ambrisentan
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTetracycline Hydrochloride NDC 0591-2474
- Generic Name
- Tetracycline Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Tetracycline Hydrochloride
- Dosage Form
- Capsule
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Tetracycline Hydrochloride
- Dosage Form
- Capsule
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugTetracycline Hydrochloride NDC 0591-2475
- Generic Name
- Tetracycline Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBudesonide NDC 0591-2510
- Generic Name
- Budesonide
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Allergan, Inc.
NDC Product
Human Prescription DrugTaytulla NDC 0023-5862
- Generic Name
- Norethindrone Acetate And Ethinyl Estradiol, And Ferrous Fum...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA
Active Listing
Almay
NDC Product
Human Otc DrugAlmay Clear Complexion Makeup Buff NDC 0311-0742
- Generic Name
- Salicylic Acid
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAlmay Clear Complexion Makeup Naked NDC 0311-0743
- Generic Name
- Salicylic Acid
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAlmay Clear Complexion Makeup Neutral NDC 0311-0744
- Generic Name
- Salicylic Acid
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAlmay Clear Complexion Makeup Beige NDC 0311-0745
- Generic Name
- Salicylic Acid
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAlmay Clear Complexion Makeup Sand Beige NDC 0311-0746
- Generic Name
- Salicylic Acid
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAlmay Clear Complexion Makeup Warm Beige NDC 0311-0747
- Generic Name
- Salicylic Acid
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAlmay Clear Complexion Makeup Ivory NDC 0311-0748
- Generic Name
- Salicylic Acid
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Amneal Pharmaceuticals of New York LLC
NDC Product
Human Prescription DrugCarvedilol Phosphate NDC 0115-1248
- Generic Name
- Carvedilol Phosphate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCarvedilol Phosphate NDC 0115-1249
- Generic Name
- Carvedilol Phosphate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCarvedilol Phosphate NDC 0115-1250
- Generic Name
- Carvedilol Phosphate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCarvedilol Phosphate NDC 0115-1251
- Generic Name
- Carvedilol Phosphate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
BF ASCHER AND CO INC
NDC Product
Human Otc DrugMobisyl NDC 0225-0360
- Generic Name
- Trolamine Salicylate
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Bayer HealthCare LLC.
NDC Product
Human Otc Drug- Generic Name
- Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Suc...
- Dosage Form
- Kit
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, P...
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAlka-seltzer Heartburn Reliefchews NDC 0280-0221
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAlka-seltzer Ultra Strength Heartburn Reliefchews NDC 0280-0245
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Bayer HealthCare, LLC.
NDC Product
Human Otc Drug- Generic Name
- Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Suc...
- Dosage Form
- Kit
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Church & Dwight Co., Inc.
NDC Product
Human Otc DrugZicam Cold Remedy Zinc And Elderberry Lozenge NDC 10237-462
- Generic Name
- Zinc Acetate Anhydrous, Zinc Gluconate, And Sambucus Nigra F...
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
Cosette Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugCiprofloxacin Hydrochloride And Hydrocortisone NDC 0713-0851
- Generic Name
- Ciprofloxacin Hydrochloride And Hydrocortisone
- Dosage Form
- Suspension/ Drops
- Route
- Auricular (otic)
- Marketing
- ANDA
Active Listing
Endo USA, Inc.
NDC Product
Human Prescription DrugDutasteride And Tamsulosin Hydrochloride NDC 10370-280
- Generic Name
- Dutasteride And Tamsulosin Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
Exeltis USA, Inc.
NDC Product
Human Prescription DrugVitafol One NDC 0642-0070
- Generic Name
- Prenatal Supplement With Dha
- Dosage Form
- Capsule, Gelatin Coated
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugVitafol Ultra NDC 0642-0093
- Generic Name
- Doconexent, Niacinamide, .alpha.-tocopherol Acetate, Dl-, Ch...
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugVitafol Fe Plus NDC 0642-7473
- Generic Name
- Doconexent, Niacinamide, .alpha.-tocopherol Acetate, Dl-, Ch...
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
Genentech, Inc.
NDC Product
Human Prescription DrugCellcept NDC 0004-0261
- Generic Name
- Mycophenolate Mofetil
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- NDA
Active Listing
Haleon US Holdings LLC
NDC Product
Human Otc DrugRobitussin Medi-soothers NDC 0031-9306
- Generic Name
- Dextromethorphan Hydrobromide, Menthol
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRobitussin Medi-soothers NDC 0031-9307
- Generic Name
- Dextromethorphan Hydrobromide, Menthol
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Severe Cold Relief Daytime NDC 0067-0100
- Generic Name
- Acetaminophen, Dextromethorphan Hbr
- Dosage Form
- Powder, For Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Severe Cold Relief Daytime Honey Ginger NDC 0067-0103
- Generic Name
- Acetaminophen, Dextromethorphan Hbr
- Dosage Form
- Powder, For Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Severe Cold Relief Daytime Berry Burst NDC 0067-0106
- Generic Name
- Acetaminophen, Dextromethorphan Hbr
- Dosage Form
- Powder, For Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGas-x Total Relief Maximum Strength NDC 0067-0118
- Generic Name
- Calcium Carbonate, Simethicone
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGas-x Total Relief Maximum Strength NDC 0067-0119
- Generic Name
- Calcium Carbonate, Simethicone
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Severe Cold Relief Combo Pack NDC 0067-0122
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Diphenhydramine Hcl
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Severe Cold Relief Combo Pack NDC 0067-0123
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Diphenhydramine Hcl
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGas-x Ultra Strength Antigas Softgels NDC 0067-6274
- Generic Name
- Simethicone
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGas-x Maximum Strength Softgels NDC 0067-6283
- Generic Name
- Simethicone
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Severe Cold Relief Daytime Berry Burst NDC 0067-6800
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Phenylephrine Hydrochlo...
- Dosage Form
- Powder
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Severe Cold Relief Nighttime NDC 0067-6801
- Generic Name
- Acetaminophen, Diphenhydramine Hydrochloride, Phenylephrine ...
- Dosage Form
- Powder
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Severe Cold Relief Daytime NDC 0067-6802
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Phenylephrine Hcl
- Dosage Form
- Powder, For Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Severe Cold Relief Nighttime NDC 0067-6803
- Generic Name
- Acetaminophen, Diphenhydramine Hcl, Phenylephrine Hcl
- Dosage Form
- Powder, For Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Phenylephrine Hcl, Diph...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Flu Relief Max Strength Daytime NDC 0067-7921
- Generic Name
- Acetaminophen, Dextromethorphan Hbr
- Dosage Form
- Powder
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Flu Relief Max Strength Nighttime NDC 0067-7922
- Generic Name
- Acetaminophen, Chlorpheniramine Maleate, Dextromethorphan Hb...
- Dosage Form
- Powder
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Acetaminophen, Dextromethorphan Hbr, And Acetaminophen, Chlo...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGas-x Ultimate Strength Softgels NDC 0067-8075
- Generic Name
- Simethicone
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugEx-lax Regular Strength Chocolated Stimulant Laxative NDC 0067-8140
- Generic Name
- Sennosides
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Phenylephrine Hcl
- Dosage Form
- Powder, For Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Acetaminophen, Diphenhydramine Hcl, Phenylephrine Hcl
- Dosage Form
- Powder, For Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Chewy Bites NDC 0135-0183
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Chewy Bites Berry Shake NDC 0135-0184
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Chewy Bites Tropical Fruit Smoothie NDC 0135-0185
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Chewy Bites Raspberry Lemonade NDC 0135-0188
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Chewy Delights NDC 0135-0560
- Generic Name
- Calcium Carbonate
- Dosage Form
- Bar, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Chewy Delights NDC 0135-0561
- Generic Name
- Calcium Carbonate
- Dosage Form
- Bar, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Chewy Delights NDC 0135-0569
- Generic Name
- Calcium Carbonate
- Dosage Form
- Bar, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Chewy Bites NDC 0135-0606
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugPanadol Cold And Flu Nondrowsy NDC 0135-0607
- Generic Name
- Acetaminophen And Phenyleprine Hcl
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Chewy Bites NDC 0135-0618
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Chewy Bites Peppermint NDC 0135-0623
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Chewy Bites With Gas Relief NDC 0135-0624
- Generic Name
- Calcium Carbonate And Simethicone
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Chewy Bites Mixed Fruit NDC 0135-0641
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Chewy Bites Orange And Cream Es NDC 0135-0642
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAdvil NDC 0573-0149
- Generic Name
- Ibuprofen
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugAdvil NDC 0573-0169
- Generic Name
- Ibuprofen
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugAdvil Multi-symptom Cold And Flu NDC 0573-0190
- Generic Name
- Chlorpheniramine Maleate, Ibuprofen, Phenylephrine Hcl
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugAdvil NDC 0573-1769
- Generic Name
- Ibuprofen
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- NDA
Active Listing
Hikma Pharmaceuticals USA Inc
NDC Product
Human Prescription DrugProgesterone NDC 0054-0829
- Generic Name
- Progesterone
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugProgesterone NDC 0054-0830
- Generic Name
- Progesterone
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
KVK-TECH, Inc.
NDC Product
Human Prescription DrugCyclobenzaprine Hydrochloride NDC 10702-006
- Generic Name
- Cyclobenzaprine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCyclobenzaprine Hydrochloride NDC 10702-007
- Generic Name
- Cyclobenzaprine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Kao USA Inc.
NDC Product
Human Otc DrugHello Sunday The Mineral One Lightweight Serum Spf 50 NDC 10596-804
- Generic Name
- Zinc Oxide
- Dosage Form
- Emulsion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugHello Sunday The Shimmer One Mineral Glow Spf 45 NDC 10596-805
- Generic Name
- Zinc Oxide
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Lannett Company, Inc.
NDC Product
Human Prescription DrugEntacapone NDC 0527-1830
- Generic Name
- Entacapone
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFluvastatin Sodium NDC 0527-2580
- Generic Name
- Fluvastatin Sodium
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDronabinol NDC 0527-4125
- Generic Name
- Dronabinol
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMycophenolate Mofetil NDC 0527-5160
- Generic Name
- Mycophenolate Mofetil
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
Major Pharmaceuticals
NDC Product
Human Prescription DrugTretinoin NDC 0904-6867
- Generic Name
- Tretinoin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugCold And Flu Relief Daytime NDC 0904-6995
- Generic Name
- Acetaminohpen, Dextromethorphan Hbr, Phenylephrine Hcl
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugNight Time Cold And Flu Relief NDC 0904-6996
- Generic Name
- Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Suc...
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Prescription DrugNifedipine NDC 0904-7082
- Generic Name
- Nifedipine
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBenzonatate NDC 0904-7153
- Generic Name
- Benzonatate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFenofibrate NDC 0904-7161
- Generic Name
- Fenofibrate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 0904-7262
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 0904-7263
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugStool Softener Laxative NDC 0904-7281
- Generic Name
- Docusate Sodium
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Prescription DrugFenofibrate NDC 0904-7539
- Generic Name
- Fenofibrate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Marlex Pharmaceuticals, Inc
NDC Product
Human Prescription DrugLacosamide NDC 10135-799
- Generic Name
- Lacosamide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLacosamide NDC 10135-800
- Generic Name
- Lacosamide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLacosamide NDC 10135-801
- Generic Name
- Lacosamide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLacosamide NDC 10135-802
- Generic Name
- Lacosamide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Mylan Pharmaceuticals Inc.
NDC Product
Human Prescription DrugCimetidine NDC 0378-0053
- Generic Name
- Cimetidine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCimetidine NDC 0378-0317
- Generic Name
- Cimetidine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCimetidine NDC 0378-0372
- Generic Name
- Cimetidine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCimetidine NDC 0378-0541
- Generic Name
- Cimetidine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFenofibrate NDC 0378-3065
- Generic Name
- Fenofibrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFenofibrate NDC 0378-3066
- Generic Name
- Fenofibrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEletriptan Hydrobromide NDC 0378-4287
- Generic Name
- Eletriptan Hydrobromide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEletriptan Hydrobromide NDC 0378-4288
- Generic Name
- Eletriptan Hydrobromide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Atorvastatin NDC 0378-4513
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Atorvastatin NDC 0378-4514
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Atorvastatin NDC 0378-4515
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Atorvastatin NDC 0378-4516
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Atorvastatin NDC 0378-4517
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Atorvastatin NDC 0378-4518
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Atorvastatin NDC 0378-4519
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Atorvastatin NDC 0378-4520
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NCS HealthCare of KY, LLC dba Vangard Labs
NDC Product
Human Prescription DrugFenofibrate NDC 0615-8530
- Generic Name
- Fenofibrate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFamotidine NDC 0615-8558
- Generic Name
- Famotidine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFamotidine NDC 0615-8559
- Generic Name
- Famotidine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPotassium Chloride NDC 0615-8570
- Generic Name
- Potassium Chloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 0615-8588
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Novartis Pharmaceuticals Corporation
NDC Product
Human Prescription DrugKisqali NDC 0078-0860
- Generic Name
- Ribociclib
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugKisqali NDC 0078-0867
- Generic Name
- Ribociclib
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugKisqali NDC 0078-0874
- Generic Name
- Ribociclib
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugScemblix NDC 0078-1091
- Generic Name
- Asciminib
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugScemblix NDC 0078-1098
- Generic Name
- Asciminib
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
Par Health USA, LLC
NDC Product
Human Prescription DrugTretinoin NDC 10370-268
- Generic Name
- Tretinoin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
Par Pharmaceutical Inc.
NDC Product
Human Prescription DrugOmega-3-acid Ethyl Esters NDC 0254-3010
- Generic Name
- Omega-3-acid Ethyl Esters
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
Pfizer Laboratories Div Pfizer Inc
NDC Product
Human Prescription DrugToviaz NDC 0069-0242
- Generic Name
- Fesoterodine Fumarate
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugToviaz NDC 0069-0244
- Generic Name
- Fesoterodine Fumarate
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
REESE PHARMACEUTICAL CO.
NDC Product
Human Otc DrugPinworm Medicine NDC 10956-778
- Generic Name
- Pyrantel Pamoate
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
REVLON
NDC Product
Human Otc DrugCeramide Lift And Firm NDC 10967-666
- Generic Name
- Octinoxate, Oxybenzone, Avobenzone, Octisalate, Octocrylene
- Dosage Form
- Emulsion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugCeramide Makeup Spf 15 NDC 10967-668
- Generic Name
- Octinoxate, Titanium Dioxide
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugPrevage City Smart NDC 10967-670
- Generic Name
- Titanium Dioxide, Zinc Oxide
- Dosage Form
- Emulsion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
REVLON CONSUMER PR Consumer Products Corp
NDC Product
Human Otc DrugRv Illuminance Serum Tint Broad Spectrum 15 NDC 10967-690
- Generic Name
- Face Foundation With Spf
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRv Illuminance Serum Tint Broad Spectrum 15 Amber NDC 10967-691
- Generic Name
- Face Foundation With Spf
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRv Illuminance Serum Tint Broad Spectrum 15 Amber NDC 10967-693
- Generic Name
- Face Foundation With Spf
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRv Illuminance Serum Tint Broad Spectrum 15 Buff Beige NDC 10967-694
- Generic Name
- Face Foundation With Spf
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRv Illuminance Serum Tint Broad Spectrum 15 Cool Beige NDC 10967-695
- Generic Name
- Face Foundation With Spf
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Face Foundation With Spf
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRv Illuminance Serum Tint Broad Spectrum 15 Hazel NDC 10967-697
- Generic Name
- Face Foundation With Spf
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRv Illuminance Serum Tint Broad Spectrum 15 Light Beige NDC 10967-698
- Generic Name
- Face Foundation With Spf
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Face Foundation With Spf
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRv Illuminance Serum Tint Broad Spectrum 15 Light Tan NDC 10967-700
- Generic Name
- Face Foundation With Spf
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Face Foundation With Spf
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRv Illuminance Serum Tint Broad Spectrum 15 Rich Sand NDC 10967-702
- Generic Name
- Face Foundation With Spf
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRv Illuminance Serum Tint Broad Spectrum 15 Sandalwood NDC 10967-703
- Generic Name
- Face Foundation With Spf
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRv Illuminance Serum Tint Broad Spectrum 15 Soft Nutmeg NDC 10967-704
- Generic Name
- Face Foundation With Spf
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRv Illuminance Serum Tint Broad Spectrum 15 Tan Sand NDC 10967-705
- Generic Name
- Face Foundation With Spf
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Revlon
NDC Product
Human Otc DrugRevlon Colorstay Light Cover Foundation NDC 10967-663
- Generic Name
- Homosalate, Octisalate, Octocrylene, Titanium Dioxide,zinc O...
- Dosage Form
- Emulsion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugPrevage Anti-aging Eye Cream Spf 15 NDC 10967-685
- Generic Name
- Octinoxate, Oxybenzone
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Revlon Consumer Products Corp
NDC Product
Human Otc DrugRevlon Photoready Bb Cream Skin Perfector NDC 10967-623
- Generic Name
- Octinoxate, Octisalate, Titanium Dioxide Make-up
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRevlon Photoready Insta-fix Makeup NDC 10967-631
- Generic Name
- Titanium Dioxide, Zinc Oxide
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Sandoz Inc
NDC Product
Human Prescription DrugAzithromycin NDC 0781-8089
- Generic Name
- Azithromycin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAzithromycin NDC 0781-8090
- Generic Name
- Azithromycin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAzithromycin NDC 0781-8091
- Generic Name
- Azithromycin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMacitentan NDC 0781-8135
- Generic Name
- Macitentan
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
TEVA PHARMACEUTICALS, INC.
NDC Product
Human Prescription DrugDiclofenac Potassium NDC 0480-9435
- Generic Name
- Diclofenac Potassium
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- ANDA
Active Listing
Teva Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugFidaxomicin NDC 0480-2596
- Generic Name
- Fidaxomicin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLubiprostone NDC 0480-3479
- Generic Name
- Lubiprostone
- Dosage Form
- Capsule, Gelatin Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLubiprostone NDC 0480-4138
- Generic Name
- Lubiprostone
- Dosage Form
- Capsule, Gelatin Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
The Mentholatum Company
NDC Product
Human Otc DrugOxy Volcanic Clay Acne Wash NDC 10742-8338
- Generic Name
- Salicylic Acid
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Ultraceuticals Pty Ltd
NDC Product
Human Otc Drug- Generic Name
- Zinc Oxide
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
WALGREEN COMPANY
NDC Product
Human Otc Drug- Generic Name
- Avobenzone, Homosalate, Octisalate, Octocrylene
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugMiconazole 1 Walgreens NDC 0363-5211
- Generic Name
- Miconazole Nitrate
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA
Active Listing
WALGREENS
NDC Product
Human Otc DrugAcetaminophen NDC 0363-9538
- Generic Name
- Acetaminophen
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Walgreen Company
NDC Product
Human Otc DrugNasal Decongestant Pe NDC 0363-4531
- Generic Name
- Phenylephrine Hcl
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSinus Pe Congestion NDC 0363-4534
- Generic Name
- Diphenhydramine Hcl, Phenylephrine Hcl
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugFlu Hbp Maximum Strength NDC 0363-7380
- Generic Name
- Acetaminophen, Chlorpheniramine Maleate, Dextromethorphan Hb...
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Walgreens
NDC Product
Human Otc DrugWalgreens Pinworm Medicine NDC 0363-0618
- Generic Name
- Pyrantel Pamoate
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugNaproxen Sodium NDC 0363-0748
- Generic Name
- Naproxen Sodium
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugWal Som Nighttime Sleep Aid NDC 0363-0816
- Generic Name
- Diphenhydramine Hcl
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugStool Softener Laxative NDC 0363-4100
- Generic Name
- Docusate Sodium
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugStool Softener Laxative NDC 0363-4202
- Generic Name
- Docusate Sodium
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugChocolated Laxative NDC 0363-5000
- Generic Name
- Sennosides Stimulant Laxative
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAllergy Relief NDC 0363-9024
- Generic Name
- Diphenhydramine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Walgreens Co
NDC Product
Human Otc DrugSennosides NDC 0363-9990
- Generic Name
- Sennosides
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
