FEXOFENADINE HYDROCHLORIDE
- Product NDC
- 72476-121
- 11-digit product format
- 724760121
- Labeler code
- 72476
- Product ID
- 72476-121_af8425e2-7318-88b7-e053-2995a90a3c1f
- 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
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72476-121-30 | FEXOFENADINE HYDROCHLORIDE | 30 in 1 BOTTLE | TABLET | 30 | | 1 |
| 72476-121-30 | FEXOFENADINE HYDROCHLORIDE | 1 in 1 CARTON | TABLET | 1 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72476-121 | FEXOFENADINE HYDROCHLORIDE TABLET [RETAIL BUSINESS SERVICES, LLC] | 1 | Legacy NDC, 2 package rows | 20200918_af8425e2-7317-88b7-e053-2995a90a3c1f.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 72476-121-30 | 72476012130 | 30 in 1 BOTTLE | Historical |