NDC 55154-5399 – Cetirizine Hydrochloride
Cetirizine Hydrochloride 10 mg/1 · Tablet, Film Coated · Oral
Product NDC55154-5399
Product details
- Brand name
- Cetirizine Hydrochloride
- Generic name
- Cetirizine hydrochloride
- Labeler
- Cardinal Health 107, LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA076677
- Marketed since
- March 30, 2012
- Marketing end
- April 30, 2027
- Pharmacologic class
- Histamine-1 Receptor Antagonist
Active ingredients
- Cetirizine Hydrochloride 10 mg/1
Uses, dosage, side effects and warnings for Cetirizine hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 55154-5399-0 | 10 BLISTER PACK in 1 BAG (55154-5399-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK | Mar 30, 2012 |
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