Fexofenadine HCl and Pseudoephedrine HCI
- Product NDC
- 11673-032
- 11-digit product format
- 116730032
- Labeler code
- 11673
- Product ID
- 11673-032_dfc91b7a-ba7d-32f7-8ade-15541094d5ae
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Fexofenadine HCl and Pseudoephedrine HCI
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Target Brands Inc.
- Application
- ANDA076667
- Marketing category
- ANDA
- Marketing start
- 2015-03-27
- 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