NDC 47335-724 – Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride
Fexofenadine Hydrochloride 60 mg/1; Pseudoephedrine Hydrochloride 120 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC47335-724
Product details
- Brand name
- Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride
- Generic name
- Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA090818
- Marketed since
- March 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 (7)
| Package NDC | Description | Since |
|---|---|---|
| 47335-724-64 | 6 BLISTER PACK in 1 CARTON (47335-724-64) / 5 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (47335-724-60) | Mar 1, 2018 |
| 47335-724-66 | 2 BLISTER PACK in 1 CARTON (47335-724-66) / 5 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (47335-724-60) | Mar 1, 2018 |
| 47335-724-75 | 4 BLISTER PACK in 1 CARTON (47335-724-75) / 5 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (47335-724-60) | Mar 1, 2018 |
| 47335-724-83 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-724-83) | Mar 1, 2018 |
| 47335-724-94 | 1 BLISTER PACK in 1 CARTON (47335-724-94) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK | Mar 1, 2018 |
| 47335-724-95 | 3 BLISTER PACK in 1 CARTON (47335-724-95) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK | Mar 1, 2018 |
| 47335-724-99 | 2 BLISTER PACK in 1 CARTON (47335-724-99) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK | Mar 1, 2018 |
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