NDC 10135-762 – Cetirizine Hydrochloride
Cetirizine Hydrochloride 10 mg/1 · Tablet · Oral
Product NDC10135-762
Product details
- Brand name
- Cetirizine Hydrochloride
- Generic name
- Cetirizine Hydrochloride
- Labeler
- Marlex Pharmaceuticals, Inc
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA077498
- Marketed since
- October 1, 2022
- 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 (5)
| Package NDC | Description | Since |
|---|---|---|
| 10135-762-01 | 100 TABLET in 1 BOTTLE (10135-762-01) | Oct 1, 2022 |
| 10135-762-03 | 300 TABLET in 1 BOTTLE (10135-762-03) | Oct 1, 2022 |
| 10135-762-05 | 500 TABLET in 1 BOTTLE (10135-762-05) | Oct 1, 2022 |
| 10135-762-30 | 30 TABLET in 1 BOTTLE (10135-762-30) | Oct 1, 2022 |
| 10135-762-90 | 90 TABLET in 1 BOTTLE (10135-762-90) | Oct 1, 2022 |
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