Fexofenadine Hydrochloride
- Product NDC
- 63629-9463
- 11-digit product format
- 636299463
- Labeler code
- 63629
- Product ID
- 63629-9463_babdd18c-238b-4c50-a0ae-655a9b633e9c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- fexofenadine hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA212971
- Marketing category
- ANDA
- Marketing start
- 2022-01-07
- Marketing end
- 0000-00-00
- Substance
- FEXOFENADINE HYDROCHLORIDE
- Active strength
- 180 mg/1
- Pharmacologic classes
- Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 63629-9463-1 | 63629946301 | 1 BOTTLE in 1 CARTON (63629-9463-1) > 100 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2022-10-31 | 0000-00-00 | No | No | Current |