NDC 55681-073 – Cetirizine Hydrochloride
Cetirizine Hydrochloride 10 mg/1 · Tablet · Oral
Product NDC55681-073
Product details
- Brand name
- Cetirizine Hydrochloride
- Generic name
- Cetirizine Hydrochloride
- Labeler
- TWIN MED, LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA209274
- Marketed since
- March 2, 2022
- Listing expires
- December 31, 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 |
|---|---|---|
| 55681-073-03 | 300 TABLET in 1 BOTTLE (55681-073-03) | Apr 1, 2026 |
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