NDC 50580-719 – Zyrtec-d
Cetirizine Hydrochloride 5 mg/1; Pseudoephedrine Hydrochloride 120 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC50580-719
Product details
- Brand name
- Zyrtec-d
- Generic name
- Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride
- Labeler
- Kenvue Brands LLC
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- NDA · NDA021150
- Marketed since
- February 28, 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 (2)
| Package NDC | Description | Since |
|---|---|---|
| 50580-719-12 | 2 BLISTER PACK in 1 CARTON (50580-719-12) / 6 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK | Feb 28, 2023 |
| 50580-719-24 | 4 BLISTER PACK in 1 CARTON (50580-719-24) / 6 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK | Feb 28, 2023 |
Other Zyrtec-d products
- 50580-728 Cetirizine Hydrochloride 5 mg/1; Pseudoephedrine Hydrochloride 120… · Tablet, Film Coated, Extended Release · Kenvue Brands LLC