FEXOFENADINE HYDROCHLORIDE
- Product NDC
- 72476-126
- 11-digit product format
- 724760126
- Labeler code
- 72476
- Product ID
- 72476-126_af84f1c1-2cf3-414b-e053-2995a90a6270
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- FEXOFENADINE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- RETAIL BUSINESS SERVICES, LLC
- Application
- ANDA210137
- Marketing category
- ANDA
- Marketing start
- 2020-09-17
- Marketing end
- 0000-00-00
- Substance
- FEXOFENADINE HYDROCHLORIDE
- Active strength
- 180 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#