NDC 83939-0003 – Cetirizine
Cetirizine Hydrochloride 10 mg/1 · Tablet, Film Coated · Oral
Product NDC83939-0003
Product details
- Brand name
- Cetirizine
- Generic name
- Cetirizine Hydrochloride
- Labeler
- VERITYRX, LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078336
- Marketed since
- November 3, 2025
- Listing expires
- December 31, 2026
- Pharmacologic class
- Histamine-1 Receptor Antagonist
Active ingredients
- Cetirizine Hydrochloride 10 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 83939-0003-0 | 50 POUCH in 1 BOX, UNIT-DOSE (83939-0003-0) / 1 TABLET, FILM COATED in 1 POUCH | Nov 3, 2025 |
| 83939-0003-2 | 50 POUCH in 1 BOX, UNIT-DOSE (83939-0003-2) / 1 TABLET, FILM COATED in 1 POUCH | Nov 3, 2025 |
| 83939-0003-3 | 100 POUCH in 1 BOX, UNIT-DOSE (83939-0003-3) / 1 TABLET, FILM COATED in 1 POUCH | Nov 3, 2025 |
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