NDC 0781-5283 – Cetirizine Hydrochloride
Cetirizine Hydrochloride 5 mg/1 · Tablet, Chewable · Oral
Product NDC0781-5283
Product details
- Brand name
- Cetirizine Hydrochloride
- Generic name
- Cetirizine Hydrochloride
- Labeler
- Sandoz Inc
- Dosage form
- Tablet, Chewable
- Route
- Oral
- Marketing category
- ANDA · ANDA078692
- Marketed since
- February 14, 2008
- Listing expires
- December 31, 2027
- 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 |
|---|---|---|
| 0781-5283-64 | 30 BLISTER PACK in 1 CARTON (0781-5283-64) / 1 TABLET, CHEWABLE in 1 BLISTER PACK (0781-5283-06) | Feb 14, 2008 |
Recalls mentioning this NDC
- D-008-2013 Oct 24, 2012 · Class III
Impurity/Degradation; exceeded impurity specification at the 8 and 15 month time points (betacyclodextrin ester 1&2)
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