NDC 58602-807 – Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride
Fexofenadine Hydrochloride 60 mg/1; Pseudoephedrine Hydrochloride 120 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC58602-807
Product details
- Brand name
- Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride
- Generic name
- Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride
- Labeler
- Aurohealth LLC
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA209116
- Marketed since
- October 30, 2017
- Listing expires
- December 31, 2027
- Pharmacologic class
- Histamine-1 Receptor Antagonist; alpha-Adrenergic Agonist
Active ingredients
- Fexofenadine Hydrochloride 60 mg/1
- Pseudoephedrine Hydrochloride 120 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 58602-807-67 | 2 BLISTER PACK in 1 CARTON (58602-807-67) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK | Oct 30, 2017 |
| 58602-807-83 | 1 BLISTER PACK in 1 CARTON (58602-807-83) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK | Oct 30, 2017 |
| 58602-807-84 | 3 BLISTER PACK in 1 CARTON (58602-807-84) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK | Oct 30, 2017 |
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