Fexofenadine HCL
- Product NDC
- 63629-7997
- 11-digit product format
- 636297997
- Labeler code
- 63629
- Product ID
- 63629-7997_602bb966-56ee-48a1-8e08-7ef94dd825d0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Fexofenadine HCL
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA204097
- Marketing category
- ANDA
- Marketing start
- 2016-08-19
- Marketing end
- 0000-00-00
- Substance
- FEXOFENADINE HYDROCHLORIDE
- Active strength
- 180 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-7997-1 | 63629799701 | 30 TABLET in 1 BOTTLE (63629-7997-1) | 30 tablet | 2019-04-11 | 0000-00-00 | No | No | Current |