NDC 45802-147 – Cetirizine hydrochloride and Pseudoephedrine hydrochloride
Cetirizine Hydrochloride 5 mg/1; Pseudoephedrine Hydrochloride 120 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC45802-147
Product details
- Brand name
- Cetirizine hydrochloride and Pseudoephedrine hydrochloride
- Generic name
- Cetirizine hydrochloride, Pseudoephedrine hydrochloride
- Labeler
- Padagis Israel Pharmaceuticals Ltd
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA210719
- Marketed since
- March 31, 2020
- Listing expires
- December 31, 2026
- Pharmacologic class
- Histamine-1 Receptor Antagonist; alpha-Adrenergic Agonist
Active ingredients
- Cetirizine Hydrochloride 5 mg/1
- Pseudoephedrine Hydrochloride 120 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 45802-147-53 | 12 BLISTER PACK in 1 CARTON (45802-147-53) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK | Mar 31, 2020 |
| 45802-147-62 | 24 BLISTER PACK in 1 CARTON (45802-147-62) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK | Mar 31, 2020 |
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