NDC 51660-939 – Cetirizine Hydrochloride
Cetirizine Hydrochloride 10 mg/1 · Tablet · Oral
Product NDC51660-939
Product details
- Brand name
- Cetirizine Hydrochloride
- Generic name
- Cetirizine Hydrochloride
- Labeler
- Ohm Laboratories Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA077498
- Marketed since
- December 27, 2007
- Listing expires
- December 31, 2026
- 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 (6)
| Package NDC | Description | Since |
|---|---|---|
| 51660-939-01 | 100 TABLET in 1 BOTTLE (51660-939-01) | Dec 27, 2007 |
| 51660-939-13 | 120 TABLET in 1 BOTTLE (51660-939-13) | Dec 27, 2007 |
| 51660-939-30 | 30 TABLET in 1 BOTTLE (51660-939-30) | Dec 27, 2007 |
| 51660-939-53 | 300 TABLET in 1 BOTTLE (51660-939-53) | Dec 27, 2007 |
| 51660-939-54 | 14 TABLET in 1 BLISTER PACK (51660-939-54) | Dec 27, 2007 |
| 51660-939-90 | 90 TABLET in 1 BOTTLE (51660-939-90) | Dec 27, 2007 |
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