NDC 58602-703 – Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride
Cetirizine Hydrochloride 5 mg/1; Pseudoephedrine Hydrochloride 120 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC58602-703
Product details
- Brand name
- Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride
- Generic name
- Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride
- Labeler
- Aurohealth LLC
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA212409
- Marketed since
- March 8, 2023
- Listing expires
- December 31, 2027
- Pharmacologic class
- Histamine-1 Receptor Antagonist; alpha-Adrenergic Agonist
Active ingredients
- Cetirizine Hydrochloride 5 mg/1
- Pseudoephedrine Hydrochloride 120 mg/1
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 58602-703-09 | 12 BLISTER PACK in 1 CARTON (58602-703-09) / 2 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK | Mar 8, 2023 |
| 58602-703-53 | 12 BLISTER PACK in 1 CARTON (58602-703-53) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK | Mar 8, 2023 |
| 58602-703-75 | 2 BLISTER PACK in 1 CARTON (58602-703-75) / 6 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK | Mar 8, 2023 |
| 58602-703-76 | 4 BLISTER PACK in 1 CARTON (58602-703-76) / 6 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK | Mar 8, 2023 |
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