NDC 0378-3635 – Cetirizine Hydrochloride
Cetirizine Hydrochloride 5 mg/1 · Tablet, Film Coated · Oral
Product NDC0378-3635
Product details
- Brand name
- Cetirizine Hydrochloride
- Generic name
- Cetirizine hydrochloride
- Labeler
- Mylan Pharmaceuticals Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA076677
- Marketed since
- December 27, 2007
- Listing expires
- December 31, 2026
- Pharmacologic class
- Histamine-1 Receptor Antagonist
Active ingredients
- Cetirizine Hydrochloride 5 mg/1
Uses, dosage, side effects and warnings for Cetirizine hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0378-3635-01 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-3635-01) | Dec 27, 2007 |
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