Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride
- Product NDC
- 62011-0376
- 11-digit product format
- 620110376
- Labeler code
- 62011
- Product ID
- 62011-0376_301d7f36-a24b-4d4e-a3a2-6cc20e634d13
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- McKESSON Corporation
- Application
- ANDA209116
- Marketing category
- ANDA
- Marketing start
- 2017-10-30
- Marketing end
- 0000-00-00
- Substance
- FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE
- Active strength
- 60 mg/1; mg/1
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record