Fexofenadine hydrochloride
- Product NDC
- 70692-134
- 11-digit product format
- 706920134
- Labeler code
- 70692
- Product ID
- 70692-134_b43fc254-c365-5e80-e053-2a95a90a799f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Fexofenadine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Strive Pharmaceuticals Inc
- Application
- ANDA211075
- Marketing category
- ANDA
- Marketing start
- 2019-07-22
- 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 |
|---|
| 70692-134-29 | Fexofenadine hydrochloride | 3 in 1 BLISTER PACK | TABLET | 3 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70692-134 | FEXOFENADINE HYDROCHLORIDE TABLET [STRIVE PHARMACEUTICALS INC] | 2 | Legacy NDC, 1 package rows | 20201117_9717c35e-cfd3-6605-e053-2995a90a1de5.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70692-134-29 | 70692013429 | 3 TABLET in 1 BLISTER PACK (70692-134-29) | 3 tablet | 2019-07-22 | 0000-00-00 | No | No | Current |