NDC Product
Human Otc DrugSkinmedica Acne Clarifying Treatment NDC 0023-1230
- Generic Name
- Salicylic Acid
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Substance Identification & Data
This profile provides standardized clinical and technical data for Xanthan Gum, uniquely identified by the FDA Unique Ingredient Identifier (UNII) TTV12P4NEE.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 11138-66-2 and the RxNorm Concept ID (RxCUI) 1307815. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
Detailed Substance Profile
Preferred Name
XANTHAN GUM
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
TTV12P4NEE
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
967771
Taxonomic Serial Number for species identified in the Integrated Taxonomic Information System.
NCBI Taxonomy
339
Unique numeric identifier used to specify biological species in the NCBI database.
Synonyms and Nomenclature
This section provides a complete list of nomenclature and identifier mappings for Xanthan 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
XANTHAN GUM
OF
Common Names & Synonyms
GUM, XANTHAN
CN
MONAD GUM DA
CN
MONAT GUM DA
CN
POLYSACCHARIDE B 1459
CN
POLYSACCHARIDE B-1459
CN
RHODIGEL-23 [II]
CN
XANTHAN
CN
XANTHAN GUM [EP MONOGRAPH]
CN
XANTHAN GUM [FCC]
CN
XANTHAN GUM [II]
CN
XANTHAN GUM [MART.]
CN
XANTHAN GUM [MI]
CN
XANTHAN GUM [VANDF]
CN
XANTHAN GUM [WHO-DD]
CN
XANTHOMONAS CAMPESTRIS BACTERIAL COAT POLYSACCHARIDE
CN
XANTHOMONAS GUM
CN
Brand / Trade Names
KELGUM
BN
KELTROL
BN
KELZAN
BN
RHODIGEL 23
BN
RHODIGEL-23
BN
RHODOPOL 23
BN
XANTURAL
BN
Technical Codes
E415
CD
E-415
CD
E-415-
CD
INS NO.415
CD
INS-415
CD
NDC Products Containing XANTHAN 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 (500), only Active Listings are currently displayed. Display is limited to the first 200 products.
Showing 200 active products
Allergan, Inc.
Active Listing
NDC Product
Human Otc DrugTotal Defense Repair Broad Spectrum Spf 34 Sunscreen NDC 0023-5494
- Generic Name
- Octinoxate, Octisalate And Zinc Oxide
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Octinoxate, Octisalate, Titanium Dioxide And Zinc Oxide
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Amneal Pharmaceuticals of New York LLC
NDC Product
Human Prescription DrugOxymorphone Hydrochloride NDC 0115-1231
- Generic Name
- Oxymorphone Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxymorphone Hydrochloride NDC 0115-1232
- Generic Name
- Oxymorphone Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxymorphone Hydrochloride NDC 0115-1233
- Generic Name
- Oxymorphone Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxymorphone Hydrochloride NDC 0115-1234
- Generic Name
- Oxymorphone Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
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
NDC Product
Human Prescription DrugOxymorphone Hydrochloride NDC 0115-1315
- Generic Name
- Oxymorphone Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxymorphone Hydrochloride NDC 0115-1316
- Generic Name
- Oxymorphone Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxymorphone Hydrochloride NDC 0115-1317
- Generic Name
- Oxymorphone Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
C.B. Fleet Company, Inc.
NDC Product
Human Otc DrugPedia-lax NDC 0132-0113
- Generic Name
- Docusate Sodium
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Colgate Oral Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugPrevident 5000 Plus Fruitastic NDC 0126-0286
- Generic Name
- Sodium Fluoride
- Dosage Form
- Paste, Dentifrice
- Route
- Dental
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugPrevident 5000 Plus Spearmint NDC 0126-0287
- Generic Name
- Sodium Fluoride
- Dosage Form
- Paste, Dentifrice
- Route
- Dental
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugPrevident Orthodefense NDC 0126-0289
- Generic Name
- Sodium Fluoride
- Dosage Form
- Paste, Dentifrice
- Route
- Dental
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugPrevident 5000 Kids NDC 0126-0311
- Generic Name
- Sodium Fluoride
- Dosage Form
- Paste, Dentifrice
- Route
- Dental
- 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
NDC Product
Human Prescription DrugTamiflu NDC 0004-0822
- Generic Name
- Oseltamivir Phosphate
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- NDA
Active Listing
Haleon US Holdings LLC
NDC Product
Human Otc Drug- Generic Name
- Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRobitussin Honey Cough Dm Day Night Value Pack NDC 0031-2059
- Generic Name
- Dextromethorphan Hbr, Guaifenesin, Doxylamine Succinate
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Dextromethorphan Hbr, Guaifenesin
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Dextromethorphan Hbr, Guaifenesin
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRobitussin Day And Night Cough Relief Value Pack NDC 0031-2099
- Generic Name
- Dextromethorphan Hydrobromide, Guaifenesin, Chlorpheniramine...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRobitussin Childrens Honey Day Night Dm Value Pack NDC 0031-2102
- Generic Name
- Dextromethorphan Hbr, Guaifenesin, Doxylamine Succinate
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRobitussin Day And Night Maximum Strength Cough Dm NDC 0031-2103
- Generic Name
- Dextromethorphan Hydrobromide, Guaifenesin, Doxylamine Succi...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRobitussin Day And Night Cough Relief Dm Max NDC 0031-2834
- Generic Name
- Dextromethorphan Hydrobromide, Guaifenesin, Doxylamine Succi...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRobitussin 12 Hour Cough Relief NDC 0031-8655
- Generic Name
- Dextromethorphan Polistirex
- Dosage Form
- Suspension, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugChildrens Robitussin Cough And Chest Congestion Dm NDC 0031-8702
- Generic Name
- Dextromethorphan Hydrobromide And Guaifenesin
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRobitussin Maximum Strength Nighttime Cough Dm NDC 0031-8718
- Generic Name
- Dextromethorphan Hydrobromide, Doxylamine Succinate
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugChildrens Robitussin 12 Hour Cough Relief NDC 0031-8725
- Generic Name
- Dextromethorphan Polistirex
- Dosage Form
- Suspension, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugChildrens Robitussin 12 Hour Cough Relief NDC 0031-8726
- Generic Name
- Dextromethorphan Polistirex
- Dosage Form
- Suspension, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Dextromethorphan Hbr, Guaifenesin
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Acetaminophen, Dextromethorphan Hydrobromide
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRobitussin Severe Multi-symptom Cough Cold Flu NDC 0031-8751
- Generic Name
- Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, P...
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRobitussin 12 Hour Cough Relief NDC 0031-8753
- Generic Name
- Dextromethorphan Polistirex
- Dosage Form
- Suspension, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugRobitussin 12 Hour Cough Relief NDC 0031-8754
- Generic Name
- Dextromethorphan Polistirex
- Dosage Form
- Suspension, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugRobitussin 12 Hour Cough Relief NDC 0031-8755
- Generic Name
- Dextromethorphan Polistirex
- Dosage Form
- Suspension, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Dextromethorphan Hbr, Guaifenesin
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRobitussin Cough Plus Chest Congestion Dm NDC 0031-8757
- Generic Name
- Dextromethorphan Hydrobromide And Guaifenesin
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Dextromethorphan Hydrobromide, Guaifenesin
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugChildrens Robitussin Honey Cough And Chest Congestion Dm NDC 0031-8760
- Generic Name
- Dextromethorphan Hbr, Guaifenesin
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Acetaminophen And Diphenhydramine Hydrochloride
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRobitussin Honey Severe Cough, Flu Plus Sore Throat NDC 0031-8771
- Generic Name
- Acetaminophen, Dextromethorphan Hbr
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Flu Relief Max Strength Daytime NDC 0067-8204
- Generic Name
- Acetaminophen, Dextromethorphan Hbr
- Dosage Form
- Syrup
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Flu Relief Max Strength Nighttime NDC 0067-8205
- Generic Name
- Acetaminophen, Chlorpheniramine Maleate, Dextromethorphan Hb...
- Dosage Form
- Syrup
- 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 DrugGaviscon NDC 0135-0094
- Generic Name
- Aluminum Hydroxide And Magnesium Carbonate
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGaviscon NDC 0135-0095
- Generic Name
- Aluminum Hydroxide And Magnesium Carbonate
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAquafresh Extreme Clean Whitening Action NDC 0135-0234
- Generic Name
- Sodium Fluoride
- Dosage Form
- Paste
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSensodyne Pronamel Mineral Boost Refreshing Peppermint NDC 0135-0450
- Generic Name
- Potassium Nitrate And Sodium Fluoride
- Dosage Form
- Paste
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSensodyne Pronamel Daily Protection NDC 0135-0460
- Generic Name
- Potassium Nitrate And Sodium Fluoride
- Dosage Form
- Paste
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSensodyne Advanced Whitening NDC 0135-0479
- Generic Name
- Potassium Nitrate
- Dosage Form
- Paste
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSensodyne Pronamel Mineral Boost Whitening Action NDC 0135-0480
- Generic Name
- Potassium Nitrate And Sodium Fluoride
- Dosage Form
- Paste
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSensodyne Pronamel Gentle Whitening NDC 0135-0484
- Generic Name
- Potassium Nitrate And Sodium Fluoride
- Dosage Form
- Paste
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSensodyne Pronamel Intensive Enamel Repair Extra Fresh NDC 0135-0486
- Generic Name
- Potassium Nitrate And Sodium Fluoride
- Dosage Form
- Paste
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSensodyne Pronamel Intensive Enamel Repair Clean Mint NDC 0135-0492
- Generic Name
- Potassium Nitrate And Sodium Fluoride
- Dosage Form
- Paste
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugNicorette NDC 0135-0508
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugNicorette NDC 0135-0510
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugNicorette NDC 0135-0511
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugSensodyne Pronamel Fresh Breath NDC 0135-0520
- Generic Name
- Potassium Nitrate And Sodium Fluoride
- Dosage Form
- Paste
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSensodyne Extra Whitening NDC 0135-0525
- Generic Name
- Potassium Nitrate And Sodium Fluoride
- Dosage Form
- Paste
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSensodyne Fresh Mint NDC 0135-0529
- Generic Name
- Potassium Nitrate And Sodium Fluoride
- Dosage Form
- Paste
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSensodyne NDC 0135-0550
- Generic Name
- Potassium Nitrate And Sodium Fluoride
- Dosage Form
- Paste
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugBiotene Fresh Mint Original NDC 0135-0557
- Generic Name
- Sodium Fluoride
- Dosage Form
- Paste
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugBiotene Gentle Mint NDC 0135-0558
- Generic Name
- Sodium Fluoride
- Dosage Form
- Paste
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSensodyne Pronamel Multi Action NDC 0135-0568
- Generic Name
- Potassium Nitrate And Sodium Fluoride
- Dosage Form
- Paste
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGaviscon NDC 0135-0574
- Generic Name
- Aluminum Hydroxide And Magnesium Carbonate
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSensodyne True White NDC 0135-0579
- Generic Name
- Potassium Nitrate And Sodium Fluoride
- Dosage Form
- Paste
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSensodyne Pronamel Gentle Whitening Advanced NDC 0135-0580
- Generic Name
- Potassium Nitrate And Sodium Fluoride
- Dosage Form
- Paste
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSensodyne True White NDC 0135-0581
- Generic Name
- Potassium Nitrate And Sodium Fluoride
- Dosage Form
- Paste
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAquafresh Cavity Protection NDC 0135-0590
- Generic Name
- Sodium Fluoride
- Dosage Form
- Paste
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAquafresh Extra Fresh Plus Whitening NDC 0135-0591
- Generic Name
- Sodium Fluoride
- Dosage Form
- Paste
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSensodyne NDC 0135-0593
- Generic Name
- Potassium Nitrate And Sodium Fluoride
- Dosage Form
- Paste
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSensodyne Pronamel Strong And Bright Enamel Mint NDC 0135-0602
- Generic Name
- Potassium Nitrate And Sodium Fluoride
- Dosage Form
- Paste
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSensodyne Pronamel Strong And Bright Enamel Extra Fresh NDC 0135-0603
- Generic Name
- Potassium Nitrate And Sodium Fluoride
- Dosage Form
- Paste
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAquafresh Extreme Clean Pure Breath Action NDC 0135-0604
- Generic Name
- Sodium Fluoride
- Dosage Form
- Paste
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAquafresh Sensitive Maximum Strength NDC 0135-0605
- Generic Name
- Potassium Nitrate And Sodium Fluoride
- Dosage Form
- Paste
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugNicorette NDC 0135-0625
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugNicorette NDC 0135-0626
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugNicorette NDC 0135-0635
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicorette NDC 0135-0636
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugSensodyne Extra Whitening Cool Mint NDC 0135-0643
- Generic Name
- Potassium Nitrate And Sodium Fluoride
- Dosage Form
- Paste
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSensodyne Pronamel Gentle Whitening Fresh Mint NDC 0135-0644
- Generic Name
- Potassium Nitrate And Sodium Fluoride
- Dosage Form
- Paste
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSensodyne Pronamel Active Shield Fresh Mint NDC 0135-0700
- Generic Name
- Potassium Nitrate And Sodium Fluoride
- Dosage Form
- Paste
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSensodyne Pronamel Active Shield Cool Mint NDC 0135-0701
- Generic Name
- Potassium Nitrate And Sodium Fluoride
- Dosage Form
- Paste
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSensodyne Clinical White Stain Protector NDC 0135-0702
- Generic Name
- Potassium Nitrate, Sodium Fluoride
- Dosage Form
- Paste
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSensodyne Clinical White Enamel Strengthening NDC 0135-0703
- Generic Name
- Potassium Nitrate, Sodium Fluoride
- Dosage Form
- Paste
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSensodyne Pronamel Kids Bubble Twist NDC 0135-0808
- Generic Name
- Sodium Fluoride
- Dosage Form
- Paste
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSensodyne Pronamel Kids Berry Twist NDC 0135-0809
- Generic Name
- Sodium Fluoride
- Dosage Form
- Paste
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSensodyne Pronamel Clinical Enamel Strength Deep Clean NDC 0135-0810
- Generic Name
- Potassium Nitrate, Sodium Fluoride
- Dosage Form
- Paste
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Potassium Nitrate, Sodium Fluoride
- Dosage Form
- Paste
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSensodyne Pronamel Kids Bubble Mint NDC 0135-0818
- Generic Name
- Sodium Fluoride
- Dosage Form
- Paste, Dentifrice
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugNatean Clean And Whiten NDC 0135-1200
- Generic Name
- Sodium Fluoride
- Dosage Form
- Paste
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugNatean Clean Plus Sensitivity Relief NDC 0135-1250
- Generic Name
- Potassium Nitrate, Sodium Fluoride
- Dosage Form
- Paste
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugNicorette NDC 0135-1500
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugNicorette NDC 0135-2800
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugSensodyne Cavity And Sensitivity NDC 0135-4032
- Generic Name
- Potassium Nitrate, Sodium Fluoride
- Dosage Form
- Paste, Dentifrice
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSensodyne Nourish Gently Soothing NDC 0135-5026
- Generic Name
- Potassium Nitrate And Sodium Fluoride
- Dosage Form
- Paste
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSensodyne Nourish Healthy White NDC 0135-5027
- Generic Name
- Potassium Nitrate And Sodium Fluoride
- Dosage Form
- Paste
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSensodyne Natural White NDC 0135-5028
- Generic Name
- Potassium Nitrate And Sodium Fluoride
- Dosage Form
- Paste
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSensodyne Advanced Whitening Plus NDC 0135-5029
- Generic Name
- Potassium Nitrate
- Dosage Form
- Paste
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSensodyne Pronamel Gentle Whitening Advanced Plus NDC 0135-5030
- Generic Name
- Potassium Nitrate, Sodium Fluoride
- Dosage Form
- Paste
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSensodyne Clinical White Intensive Clean NDC 0135-5468
- Generic Name
- Potassium Nitrate, Sodium Fluoride
- Dosage Form
- Paste
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSensodyne Pronamel Clinical Enamel Strength Fresh Breath NDC 0135-7753
- Generic Name
- Potassium Nitrate, Sodium Fluoride
- Dosage Form
- Paste, Dentifrice
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugNicorette Peppermint NDC 0135-8050
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugNicorette Peppermint NDC 0135-8060
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugNicorette Cherry Peppermint NDC 0135-8070
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugNicorette Cherry Peppermint NDC 0135-8071
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- NDA
Active Listing
Hikma Pharmaceuticals USA Inc.
NDC Product
Human Prescription DrugLinezolid NDC 0054-0319
- Generic Name
- Linezolid
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMercaptopurine NDC 0054-0879
- Generic Name
- Mercaptopurine
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
L. Perrigo Company
NDC Product
Human Otc DrugGood Sense Ibuprofen Infants NDC 0113-0057
- Generic Name
- Ibuprofen
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Ibuprofen Childrens NDC 0113-0166
- Generic Name
- Ibuprofen
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Nicotine NDC 0113-0344
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Cough Dm NDC 0113-0384
- Generic Name
- Dextromethorphan Polistirex
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
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
NDC Product
Human Otc DrugGood Sense Severe Daytime Cold And Flu NDC 0113-0603
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Guaifenesin, Phenylephr...
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Daytime Non Drowsy Cold And Flu NDC 0113-0656
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Phenylephrine Hcl
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Ibuprofen Childrens NDC 0113-0660
- Generic Name
- Ibuprofen
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Ibuprofen NDC 0113-0685
- Generic Name
- Ibuprofen
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Nicotine NDC 0113-0734
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Severe Nighttime Cold And Flu NDC 0113-0763
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Doxylamine Succinate, P...
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Nicotine NDC 0113-0873
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Ibuprofen Childrens NDC 0113-0897
- Generic Name
- Ibuprofen
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Tussin Dm Max NDC 0113-0927
- Generic Name
- Dextromethorphan Hbr, Guaifenesin
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Hemorrhoidal Maximum Strength Pain Relief NDC 0113-0944
- Generic Name
- Glycerin, Phenylephrine Hcl, Pramoxine Hcl, White Petrolatum
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Nicotine NDC 0113-0957
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Cough Dm NDC 0113-0958
- Generic Name
- Dextromethorphan Polistirex
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Nicotine NDC 0113-1125
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Nicotine NDC 0113-1190
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Antidiarrheal NDC 0113-1645
- Generic Name
- Loperamide Hcl
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Tussin Dm NDC 0113-1725
- Generic Name
- Dextromethorphan Hydrobromide, Guaifenesin
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Tussin NDC 0113-2009
- Generic Name
- Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Day Time Cold And Flu NDC 0113-2299
- Generic Name
- Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, P...
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Night Time Cold And Flu NDC 0113-2501
- Generic Name
- Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Suc...
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Nicotine NDC 0113-2502
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Nicotine NDC 0113-5023
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Night Time NDC 0113-6012
- Generic Name
- Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Suc...
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Nicotine NDC 0113-7020
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Nicotine NDC 0113-7031
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Nicotine NDC 0113-7999
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
Merck Sharp & Dohme LLC
NDC Product
Human Prescription DrugNoxafil NDC 0085-1328
- Generic Name
- Posaconazole
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugNoxafil NDC 0085-2224
- Generic Name
- Posaconazole
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugNoxafil NDC 0085-4324
- Generic Name
- Posaconazole
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugNoxafil NDC 0085-4331
- Generic Name
- Posaconazole
- Dosage Form
- Solution
- Route
- Intravenous
- Marketing
- NDA
Active Listing
Novartis Pharmaceuticals Corporation
NDC Product
Human Prescription DrugTegretol NDC 0078-0508
- Generic Name
- Carbamazepine
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTegretol NDC 0078-0509
- Generic Name
- Carbamazepine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTegretol Xr NDC 0078-0510
- Generic Name
- Carbamazepine
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTegretol Xr NDC 0078-0511
- Generic Name
- Carbamazepine
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTegretol Xr NDC 0078-0512
- Generic Name
- Carbamazepine
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugPromacta NDC 0078-0697
- Generic Name
- Eltrombopag Olamine
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- NDA
Active Listing
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 DrugPromacta NDC 0078-0972
- Generic Name
- Eltrombopag Olamine
- Dosage Form
- Powder, For Suspension
- 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
PAI Holdings, LLC dba PAI Pharma
NDC Product
Human Otc DrugCalcium Carbonate NDC 0121-0766
- Generic Name
- Calcium Carbonate
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugChildrens Ibuprofen Oral Suspension NDC 0121-0833
- Generic Name
- Ibuprofen
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugAcetaminophen NDC 0121-0941
- Generic Name
- Acetaminophen
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Prescription DrugAtovaquone NDC 0121-0956
- Generic Name
- Atovaquone
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugDye Free Childrens Acetaminophen NDC 0121-0966
- Generic Name
- Acetaminophen
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Prescription DrugAtovaquone NDC 0121-1016
- Generic Name
- Atovaquone
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugDye Free Childrens Ibuprofen NDC 0121-1022
- Generic Name
- Ibuprofen
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugChildrens Ibuprofen Oral Suspension NDC 0121-1666
- Generic Name
- Ibuprofen
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugChildrens Acetaminophen NDC 0121-1781
- Generic Name
- Acetaminophen
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAcetaminophen NDC 0121-1882
- Generic Name
- Acetaminophen
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAcetaminophen NDC 0121-2823
- Generic Name
- Acetaminophen
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugCalcium Carbonate NDC 0121-4766
- Generic Name
- Calcium Carbonate
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Person and Covey
NDC Product
Human Otc DrugSolbar Shield Spf40 NDC 0096-0682
- Generic Name
- Solbar Shield Spf40
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSolbar Zinc Spf38 NDC 0096-0688
- Generic Name
- Solbar Zinc Spf38
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSolbar Sunscreen 40 Zinc NDC 0096-0691
- Generic Name
- Sunscreen
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSolbar Sunscreen 40 Shield NDC 0096-0692
- Generic Name
- Sunscreen
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAquanil Hc NDC 0096-0732
- Generic Name
- Hydrocortisone
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAquanil Hc NDC 0096-0810
- Generic Name
- Hydrocortisone
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Pfizer Laboratories Div Pfizer Inc
NDC Product
Human Prescription DrugZithromax NDC 0069-3120
- Generic Name
- Azithromycin Dihydrate
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugZithromax NDC 0069-3130
- Generic Name
- Azithromycin Dihydrate
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugZithromax NDC 0069-3140
- Generic Name
- Azithromycin Dihydrate
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugZithromax NDC 0069-4061
- Generic Name
- Azithromycin Dihydrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
Pharmaceutical Associates, Inc.
NDC Product
Human Otc DrugChildrens Ibuprofen Oral Suspension NDC 0121-0914
- Generic Name
- Ibuprofen
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
Pharmacia & Upjohn Company LLC
NDC Product
Human Prescription DrugZyvox NDC 0009-5136
- Generic Name
- Linezolid
- Dosage Form
- Granule, For Suspension
- Route
- Oral
- Marketing
- NDA
Active Listing
Teva Pharmaceuticals USA, Inc.
NDC Product
Human Prescription DrugAzithromycin NDC 0093-2026
- Generic Name
- Azithromycin
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAzithromycin NDC 0093-2027
- Generic Name
- Azithromycin
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin NDC 0093-2267
- Generic Name
- Amoxicillin
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin NDC 0093-2268
- Generic Name
- Amoxicillin
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin And Clavulanate Potassium NDC 0093-2277
- Generic Name
- Amoxicillin And Clavulanate Potassium
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin And Clavulanate Potassium NDC 0093-2279
- Generic Name
- Amoxicillin And Clavulanate Potassium
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugImiquimod NDC 0093-3133
- Generic Name
- Imiquimod
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugCefdinir NDC 0093-4136
- Generic Name
- Cefdinir
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCefdinir NDC 0093-4137
- Generic Name
- Cefdinir
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin NDC 0093-4155
- Generic Name
- Amoxicillin
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCephalexin NDC 0093-4175
- Generic Name
- Cephalexin
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCephalexin NDC 0093-4177
- Generic Name
- Cephalexin
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOseltamivir Phosphate NDC 0093-8180
- Generic Name
- Oseltamivir Phosphate
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin And Clavulanate Potassium NDC 0093-8675
- Generic Name
- Amoxicillin And Clavulanate Potassium
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
Xttrium Laboratories, Inc.
NDC Product
Human Prescription DrugMegestrol Acetate NDC 0116-4011
- Generic Name
- Megestrol Acetate
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
