NDC 70692-139 – Cetirizine hydrochloride
Cetirizine Hydrochloride 10 mg/1 · Tablet · Oral
Product NDC70692-139
Product details
- Brand name
- Cetirizine hydrochloride
- Generic name
- Cetirizine hydrochloride
- Labeler
- Strive Pharmaceuticals Inc
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA209274
- Marketed since
- July 1, 2020
- 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 (1)
| Package NDC | Description | Since |
|---|---|---|
| 70692-139-14 | 14 TABLET in 1 BOTTLE (70692-139-14) | Jul 1, 2020 |
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