Fex-Allergy Relief
- Product NDC
- 72090-061
- 11-digit product format
- 720900061
- Labeler code
- 72090
- Product ID
- 72090-061_b078c242-b8b6-51a0-e053-2a95a90a6b06
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Fexofenadine HCl
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Pioneer Life Sciences, LLC
- Application
- ANDA204097
- Marketing category
- ANDA
- Marketing start
- 2020-09-21
- 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 Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72090-061 | FEX-ALLERGY RELIEF (FEXOFENADINE HCL) TABLET [PIONEER LIFE SCIENCES, LLC] | 1 | Legacy NDC | 20200930_b078c242-b8b5-51a0-e053-2a95a90a6b06.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72090-061-90 | 72090006190 | 90 TABLET in 1 BOTTLE (72090-061-90) | 90 tablet | 2020-09-21 | 0000-00-00 | No | No | Current |