NDC Product
Human Prescription DrugCefdinir NDC 50090-2735
- Generic Name
- Cefdinir
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
Substance Identification & Data
This profile provides standardized clinical and technical data for Guar Gum, uniquely identified by the FDA Unique Ingredient Identifier (UNII) E89I1637KE.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 9000-30-0 and the RxNorm Concept ID (RxCUI) 26344. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
Detailed Substance Profile
Preferred Name
GUAR GUM
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
E89I1637KE
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
506245
Taxonomic Serial Number for species identified in the Integrated Taxonomic Information System.
NCBI Taxonomy
3832
Unique numeric identifier used to specify biological species in the NCBI database.
USDA PLANTS ID
CYTE11
Botanical identifier maintained by the U.S. Department of Agriculture.
GRIN Nomen ID
12701
Identifier from the Germplasm Resources Information Network botanical database.
MPNS Record
WCS-2748971
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 Guar Gum. 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.
FDA Official Name
CYAMOPSIS TETRAGONOLOBA (GUAR) GUM
OF
Common Names & Synonyms
CYAMOPSIS TETRAGONOLOBA
CN
CYAMOPSIS TETRAGONOLOBA [WHO-DD]
CN
CYAMOPSIS TETRAGONOLOBA GUM [WHO-DD]
CN
CYAMOPSIS TETRAGONOLOBUS
CN
GUAR FLOUR
CN
GUAR GUM
CN
GUAR GUM [FCC]
CN
GUAR GUM [FHFI]
CN
GUAR GUM [HSDB]
CN
GUAR GUM [II]
CN
GUAR GUM [MART.]
CN
GUAR GUM [MI]
CN
GUAR GUM [VANDF]
CN
GUARAN
CN
GUARAN [MI]
CN
GUM-CYAMOPSIS
CN
Systematic Nomenclature
CYAMOPSIS TETRAGONOLOBA GUM
SYS
Technical Codes
E-412
CD
FEMA NO. 2537
CD
INS NO.412
CD
INS-412
CD
NDC Products Containing GUAR GUM
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 (259), only Active Listings are currently displayed.
Showing 174 active products
A-S Medication Solutions
Active Listing
NDC Product
Human Prescription DrugCefdinir NDC 50090-3723
- Generic Name
- Cefdinir
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCefdinir NDC 50090-4258
- Generic Name
- Cefdinir
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCefdinir NDC 50090-5811
- Generic Name
- Cefdinir
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCefdinir NDC 50090-6171
- Generic Name
- Cefdinir
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCefdinir NDC 50090-6417
- Generic Name
- Cefdinir
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCefdinir NDC 50090-7929
- Generic Name
- Cefdinir
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
Alcon Laboratories, Inc.
NDC Product
Human Otc DrugSystane Lubricant NDC 0065-0429
- Generic Name
- Polyethylene Glycol 400 And Propylene Glycol
- Dosage Form
- Solution/ Drops
- Route
- Ophthalmic
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSystane Complete NDC 0065-0481
- Generic Name
- Propylene Glycol
- Dosage Form
- Emulsion
- Route
- Ophthalmic
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSystane Ultra NDC 0065-1431
- Generic Name
- Polyethylene Glycol 400 And Propylene Glycol
- Dosage Form
- Solution/ Drops
- Route
- Ophthalmic
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSystane Ultra NDC 0065-1432
- Generic Name
- Polyethylene Glycol 400 And Propylene Glycol
- Dosage Form
- Solution/ Drops
- Route
- Ophthalmic
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSystane Balance NDC 0065-1433
- Generic Name
- Propylene Glycol
- Dosage Form
- Emulsion
- Route
- Ophthalmic
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSystane Day And Night Value Pack NDC 0065-1502
- Generic Name
- Polyethylene Glycol 400, Propylene Glycol 0.3%
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Alcon Research Ltd
NDC Product
Human Otc DrugSystane NDC 0065-0431
- Generic Name
- Polyethylene Glycol And Propylene Glycol
- Dosage Form
- Solution/ Drops
- Route
- Ophthalmic
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Amici Pharma, Inc.
NDC Product
Human Prescription DrugRisperidone NDC 69292-571
- Generic Name
- Risperidone
- Dosage Form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRisperidone NDC 69292-572
- Generic Name
- Risperidone
- Dosage Form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRisperidone NDC 69292-573
- Generic Name
- Risperidone
- Dosage Form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRisperidone NDC 69292-574
- Generic Name
- Risperidone
- Dosage Form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRisperidone NDC 69292-575
- Generic Name
- Risperidone
- Dosage Form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing
- ANDA
Active Listing
Amneal Pharmaceuticals of New York LLC
NDC Product
Human Prescription DrugMethitest NDC 0115-7037
- Generic Name
- Methyltestosterone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Aphena Pharma Solutions - Tennessee, LLC
NDC Product
Human Prescription DrugAlfuzosin Hydrochloride NDC 43353-945
- Generic Name
- Alfuzosin Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
BESTVALUE Co., Ltd
NDC Product
Human Otc DrugAn12 Skin Therapy Vita-b Aloe Soothing Gel NDC 82385-104
- Generic Name
- Glycerin
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
Best Sanitizers, Inc
NDC Product
Human Otc DrugHaccp Qe2 NDC 59900-718
- Generic Name
- Benzalkonium Chloride
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Best Sanitizers, Inc.
NDC Product
Human Otc DrugHaccp Q E2 Sanitizing NDC 59900-215
- Generic Name
- Benzalkonium Chloride
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Bryant Ranch Prepack
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 63629-1919
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 63629-1921
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 63629-1923
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 72162-1306
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
CVS Pharmacy
NDC Product
Human Otc DrugIbuprofen And Pseudoephedrine Hydrochloride NDC 59779-430
- Generic Name
- Ibuprofen And Pseudoephedrine Hydrochloride
- Dosage Form
- Tablet, Sugar Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Camber Pharmaceuticals Inc.
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 31722-926
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 31722-927
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 31722-928
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
Camber Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 31722-321
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 31722-322
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 31722-323
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 31722-324
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 31722-325
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 31722-326
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
ChemStation
NDC Product
Human Otc DrugChemstation Haccp Q E2 NDC 71212-101
- Generic Name
- Benzalkonium Chloride
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Cipla USA Inc.
NDC Product
Human Prescription DrugAlfuzosin Hydrochloride Extended Release NDC 69097-844
- Generic Name
- Alfuzosin Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLanthanum Carbonate NDC 69097-934
- Generic Name
- Lanthanum Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLanthanum Carbonate NDC 69097-935
- Generic Name
- Lanthanum Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLanthanum Carbonate NDC 69097-936
- Generic Name
- Lanthanum Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
DIRECT RX
NDC Product
Human Prescription DrugCefdinir NDC 72189-043
- Generic Name
- Cefdinir
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
Dr. Loretta, LLC
NDC Product
Human Otc DrugMicro Exfoliating Cleanser NDC 71501-1901
- Generic Name
- Salicylic Acid Soap
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Drmtlgy, LLC
NDC Product
Human Otc DrugDaydream Broad Spectrum Sunscreen Spf 40 NDC 83286-001
- Generic Name
- Zinc Oxide
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Elemis Ltd.
NDC Product
Human Otc DrugPro-collagen Skin Protection Fluid Spf 50 NDC 65912-012
- Generic Name
- Avobenzone, Homosalate, Octisalate And Octocrylene
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Exelan Pharmaceuticals Inc.
NDC Product
Human Prescription DrugAlfuzosin Hydrochloride NDC 76282-302
- Generic Name
- Alfuzosin Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Exelan Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugLanthanum Carbonate NDC 76282-476
- Generic Name
- Lanthanum Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLanthanum Carbonate NDC 76282-477
- Generic Name
- Lanthanum Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLanthanum Carbonate NDC 76282-478
- Generic Name
- Lanthanum Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
Genexa Inc.
NDC Product
Human Otc DrugGenexa Childrens Acetaminophen NDC 69676-0058
- Generic Name
- Acetaminophen
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGenexa Acetaminophen Extra Strength NDC 69676-0059
- Generic Name
- Acetaminophen
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGenexa Acetaminophen Pm Extra Strength NDC 69676-0063
- Generic Name
- Acetaminophen
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Genexa, Inc.
NDC Product
Human Otc DrugGenexa Kids Pain And Fever NDC 69676-0081
- Generic Name
- Acetaminophen
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Good Weather Inc.
NDC Product
Human Otc DrugGood Weather Skin All Over Sun Milk Face And Body Spf 50 NDC 85090-005
- Generic Name
- Zinc Oxide
- Dosage Form
- Emulsion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Granules Pharmaceuticals Inc.
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 70010-214
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 70010-215
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 70010-216
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 70010-217
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 70010-218
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 70010-219
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
Haleon US Holdings LLC
NDC Product
Human Otc DrugTums Smoothies NDC 0135-0227
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Smoothies NDC 0135-0243
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Smoothies NDC 0135-0245
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Smoothies NDC 0135-0246
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Smoothies NDC 0135-0456
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Hangzhou Bo Clean Hygiene Products Co., Ltd
NDC Product
Human Otc DrugAcne Buster NDC 78882-401
- Generic Name
- Salicylic Acid
- Dosage Form
- Patch
- Route
- Transdermal
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
Hangzhou Caring Cleaning Commodity Co., Ltd
NDC Product
Human Otc DrugAcne Buster NDC 78936-405
- Generic Name
- Salicylic Acid
- Dosage Form
- Patch
- Route
- Transdermal
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
Harrow Eye, LLC
NDC Product
Human Prescription DrugIlevro NDC 82667-400
- Generic Name
- Nepafenac
- Dosage Form
- Suspension/ Drops
- Route
- Ophthalmic
- Marketing
- NDA
Active Listing
KalVista Pharmaceuticals Ltd
NDC Product
Human Prescription DrugEkterly NDC 82928-300
- Generic Name
- Sebetralstat
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
Kenvue Brands LLC
NDC Product
Human Otc DrugTylenol Extra Strength NDC 50580-472
- Generic Name
- Acetaminophen
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
L. Perrigo Company
NDC Product
Human Otc DrugZephrex D NDC 0113-0401
- Generic Name
- Pseudoephedrine Hydrochloride
- Dosage Form
- Capsule, Gelatin Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Laser Pharmaceuticals, LLC
NDC Product
Human Prescription DrugSodium Sulfacetamide NDC 16477-410
- Generic Name
- Sodium Sulfacetamide
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
Lil' Drug Store Products, Inc
NDC Product
Human Otc DrugBc Cherry NDC 66715-9815
- Generic Name
- Aspirin And Caffeine
- Dosage Form
- Powder
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Medline Industries, LP
NDC Product
Human Otc DrugMedline NDC 53329-163
- Generic Name
- White Petrolatum, Zinc Oxide
- Dosage Form
- Ointment
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Medtech Products Inc.
NDC Product
Human Otc DrugBc Cherry NDC 63029-200
- Generic Name
- Aspirin And Caffeine
- Dosage Form
- Powder
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugBc Max NDC 63029-203
- Generic Name
- Aspirin, Acetaminophen, Caffeine
- Dosage Form
- Powder
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGoodys Cool Orange Headache NDC 63029-663
- Generic Name
- Acetaminophen And Aspirin And Caffeine
- Dosage Form
- Powder
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGoodys Extra Strength Headache Mixed Fruit Blast NDC 63029-664
- Generic Name
- Acetaminophen, Aspirin, And Caffeine
- Dosage Form
- Powder
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGoodys Hangover NDC 63029-665
- Generic Name
- Aspirin And Caffeine
- Dosage Form
- Powder
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGoodys Mental Alert NDC 63029-667
- Generic Name
- Aspirin And Caffeine
- Dosage Form
- Powder
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGoodys Max NDC 63029-668
- Generic Name
- Acetaminophen, Aspirin, And Caffeine
- Dosage Form
- Powder
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugDramamine NDC 63029-912
- Generic Name
- Meclizine Hydrochloride
- Dosage Form
- Powder
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Menper Distributors, Inc
NDC Product
Human Otc DrugDefensol-ito NDC 53145-333
- Generic Name
- Dextromethorphan, Guiafenesin, Phenylephrine
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NextWave Pharmaceuticals, Inc
NDC Product
Human Prescription DrugQuillichew Er NDC 24478-074
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Chewable, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugQuillichew Er NDC 24478-075
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Chewable, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugQuillichew Er NDC 24478-076
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Chewable, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugDyanavel Xr NDC 24478-106
- Generic Name
- Amphetamine
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugDyanavel Xr NDC 24478-108
- Generic Name
- Amphetamine
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugDyanavel Xr NDC 24478-109
- Generic Name
- Amphetamine
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugDyanavel Xr NDC 24478-110
- Generic Name
- Amphetamine
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
Novadoz Pharmaceuticals LLC
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 72205-132
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 72205-133
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 72205-134
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 72205-135
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 72205-136
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 72205-137
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
Novartis Pharmaceuticals Corporation
NDC Product
Human Prescription DrugIlevro NDC 0078-0743
- Generic Name
- Nepafenac
- Dosage Form
- Suspension/ Drops
- Route
- Ophthalmic
- Marketing
- NDA
Active Listing
NuCare Pharmaceuticals,Inc.
NDC Product
Human Prescription DrugCefdinir NDC 68071-3403
- Generic Name
- Cefdinir
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCefdinir NDC 68071-3609
- Generic Name
- Cefdinir
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCefdinir NDC 68071-4970
- Generic Name
- Cefdinir
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCefdinir NDC 68071-5106
- Generic Name
- Cefdinir
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
OHM LABORATORIES INC.
NDC Product
Human Otc DrugCetirizine Hydrochloride NDC 51660-066
- Generic Name
- Cetirizine Hydrochloride
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
Oak Essentials, LLC
NDC Product
Human Otc Drug- Generic Name
- Zinc Oxide
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Ohm Laboratories Inc.
NDC Product
Human Otc DrugIbuprofen And Pseudoephedrine Hydrochloride NDC 51660-423
- Generic Name
- Ibuprofen And Pseudoephedrine Hydrochloride
- Dosage Form
- Tablet, Sugar Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugIbuprofen And Pseudoephedrine Hydrochloride NDC 51660-490
- Generic Name
- Ibuprofen And Pseudoephedrine Hydrochloride
- Dosage Form
- Tablet, Sugar Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugIbuprofen And Pseudoephedrine Hydrochloride NDC 51660-493
- Generic Name
- Ibuprofen And Pseudoephedrine Hydrochloride
- Dosage Form
- Tablet, Sugar Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Preferred Pharmaceuticals Inc.
NDC Product
Human Prescription DrugCefdinir NDC 68788-4106
- Generic Name
- Cefdinir
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCefdinir NDC 68788-7844
- Generic Name
- Cefdinir
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCefdinir NDC 68788-8115
- Generic Name
- Cefdinir
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCefdinir NDC 68788-8655
- Generic Name
- Cefdinir
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
Private Label Skin Care
NDC Product
Human Otc DrugPhysical Daily Defense Broad Spectrum Sunscreen Spf 40 NDC 72957-009
- Generic Name
- Zinc Oxide
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Proficient Rx LP
NDC Product
Human Prescription DrugCefdinir NDC 63187-616
- Generic Name
- Cefdinir
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCefdinir NDC 63187-835
- Generic Name
- Cefdinir
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCefdinir NDC 71205-380
- Generic Name
- Cefdinir
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCefdinir NDC 71205-405
- Generic Name
- Cefdinir
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
Publix Super Markets Inc
NDC Product
Human Otc DrugIbuprofen And Pseudoephedrine Hydrochloride NDC 56062-423
- Generic Name
- Ibuprofen And Pseudoephedrine Hydrochloride
- Dosage Form
- Tablet, Sugar Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Rising Pharma Holdings, Inc.
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 64980-221
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 64980-222
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 64980-223
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
Rite-Aid
NDC Product
Human Otc DrugIbuprofen And Pseudoephedrine Hydrochloride NDC 11822-0084
- Generic Name
- Ibuprofen And Pseudoephedrine Hydrochloride
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
RoyceDerm LLC
NDC Product
Human Otc DrugRoycederm Seborrheic Dermatitis And Psoriasis Shampoo. NDC 85424-015
- Generic Name
- Salicylic Acid 3%
- Dosage Form
- Shampoo
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
SpecGx LLC
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0406-5124
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0406-5125
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0406-5126
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0406-5127
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0406-5128
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0406-5129
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
Strategic Sourcing Services LLC
NDC Product
Human Otc DrugIbuprofen And Pseudoephedrine Hydrochloride NDC 62011-0070
- Generic Name
- Ibuprofen And Pseudoephedrine Hydrochloride
- Dosage Form
- Tablet, Sugar Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Sun Pharmaceutical Industries, Inc.
NDC Product
Human Otc DrugCetirizine Hydrochloride NDC 47335-343
- Generic Name
- Cetirizine Hydrochloride
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugCetirizine Hydrochloride NDC 47335-344
- Generic Name
- Cetirizine Hydrochloride
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 57664-083
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 57664-084
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 57664-085
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 57664-086
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 57664-087
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 57664-088
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
TARGET CORPORATION
NDC Product
Human Otc DrugGas Relief - Cherry Flavor NDC 11673-066
- Generic Name
- Simethicone
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Teva Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0480-9737
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0480-9738
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0480-9739
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0480-9741
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0480-9742
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0480-9744
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
The Kind Lab, Inc.
NDC Product
Human Otc DrugFluoride Bits NDC 82976-100
- Generic Name
- Sodium Monofluorophosphate 0.76%
- Dosage Form
- Tablet
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugFluoride Bits NDC 82976-101
- Generic Name
- Sodium Monofluorophosphate 0.76%
- Dosage Form
- Tablet
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
The Kroger Company
NDC Product
Human Otc DrugIbuprofen And Pseudoephedrine Hydrochloride NDC 30142-423
- Generic Name
- Ibuprofen And Pseudoephedrine Hydrochloride
- Dosage Form
- Tablet, Sugar Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
WALGREEN COMPANY
NDC Product
Human Otc DrugIbuprofen And Pseudoephedrine Hydrochloride NDC 0363-0423
- Generic Name
- Ibuprofen And Pseudoephedrine Hydrochloride
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
WALGREENS
NDC Product
Human Otc DrugPain Reliever NDC 0363-6779
- Generic Name
- Acetaminophen
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Wasatch Product Development
NDC Product
Human Otc DrugTe-fu Recovery Massage NDC 44717-539
- Generic Name
- Menthol, Methyl Salicylate
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Welmedix LLC
NDC Product
Human Otc DrugFirst Degree Maximum Strength Burn NDC 24330-130
- Generic Name
- Pramoxine Hydrochloride
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH NOT FINAL
Active Listing
Westminster Pharmaceuticals, LLC
NDC Product
Human Prescription DrugSodium Sulfacetamide, Sulfur NDC 69367-244
- Generic Name
- Sulfacetamide Sodium And Sulfur
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugSodium Sulfacetamide And Sulfur NDC 69367-245
- Generic Name
- Sodium Sulfacetamide And Sulfur
- Dosage Form
- Suspension
- Route
- Topical
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugSodium Sulfacetamide, Sulfur NDC 69367-247
- Generic Name
- Sulfacetamide Sodium And Sulfur
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
Wisconsin Pharmacal Company
NDC Product
Human Otc DrugMg217 Psoriasis Therapeutic Scalp Treatment NDC 68093-5206
- Generic Name
- Coal Tar
- Dosage Form
- Shampoo
- Route
- Topical
- Marketing
- OTC MONOGRAPH FINAL
Active Listing
NDC Product
Human Otc DrugMg217 Psoriasis Medicated Conditioning NDC 68093-7232
- Generic Name
- Coal Tar
- Dosage Form
- Shampoo
- Route
- Topical
- Marketing
- OTC MONOGRAPH FINAL
Active Listing
XLCare Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 72865-125
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 72865-126
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 72865-127
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
