NDC 29300-313 – Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride
Cetirizine Hydrochloride 5 mg/1; Pseudoephedrine Hydrochloride 120 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC29300-313
Product details
- Brand name
- Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride
- Generic name
- Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride
- Labeler
- Unichem Pharmaceuticals (USA), Inc.
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA210507
- Marketed since
- September 10, 2024
- 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 (2)
| Package NDC | Description | Since |
|---|---|---|
| 29300-313-22 | 2 BLISTER PACK in 1 CARTON (29300-313-22) / 6 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (29300-313-61) | Jan 1, 2025 |
| 29300-313-24 | 4 BLISTER PACK in 1 CARTON (29300-313-24) / 6 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (29300-313-61) | Jan 1, 2025 |
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