NDC 71335-0300 – Cetirizine Hydrochloride
Cetirizine Hydrochloride 10 mg/1 · Tablet · Oral
Product NDC71335-0300
Product details
- Brand name
- Cetirizine Hydrochloride
- Generic name
- Cetirizine Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA077829
- Marketed since
- October 1, 2009
- 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 (9)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0300-1 | 30 TABLET in 1 BOTTLE (71335-0300-1) | Feb 16, 2018 |
| 71335-0300-2 | 14 TABLET in 1 BOTTLE (71335-0300-2) | Feb 20, 2018 |
| 71335-0300-3 | 7 TABLET in 1 BOTTLE (71335-0300-3) | Feb 9, 2022 |
| 71335-0300-4 | 10 TABLET in 1 BOTTLE (71335-0300-4) | Mar 19, 2019 |
| 71335-0300-5 | 15 TABLET in 1 BOTTLE (71335-0300-5) | Feb 9, 2022 |
| 71335-0300-6 | 90 TABLET in 1 BOTTLE (71335-0300-6) | Feb 16, 2018 |
| 71335-0300-7 | 20 TABLET in 1 BOTTLE (71335-0300-7) | Mar 7, 2019 |
| 71335-0300-8 | 60 TABLET in 1 BOTTLE (71335-0300-8) | Oct 13, 2021 |
| 71335-0300-9 | 100 TABLET in 1 BOTTLE (71335-0300-9) | May 3, 2019 |
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