NDC 37808-999 – Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride
Fexofenadine Hydrochloride 60 mg/1; Pseudoephedrine Hydrochloride 120 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC37808-999
Product details
- Brand name
- Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride
- Generic name
- Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride
- Labeler
- H E B
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA090818
- Marketed since
- August 1, 2018
- Listing expires
- December 31, 2026
- Pharmacologic class
- Histamine-1 Receptor Antagonist; alpha-Adrenergic Agonist
Active ingredients
- Fexofenadine Hydrochloride 60 mg/1
- Pseudoephedrine Hydrochloride 120 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 37808-999-30 | 1 BLISTER PACK in 1 CARTON (37808-999-30) / 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK | Aug 1, 2018 |
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