NDC 25000-220 – Cetirizine Hydrochloride Tablets, 10 mg
Cetirizine Hydrochloride 10 mg/1 · Tablet · Oral
Product NDC25000-220
Product details
- Brand name
- Cetirizine Hydrochloride Tablets, 10 mg
- Generic name
- Cetirizine Hydrochloride
- Labeler
- MARKSANS PHARMA LIMITED
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA078933
- Marketed since
- January 13, 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 Tablets,10 mg →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 25000-220-03 | 1 BOTTLE in 1 CARTON (25000-220-03) / 30 TABLET in 1 BOTTLE | Jan 13, 2022 |
| 25000-220-08 | 1 BOTTLE in 1 CARTON (25000-220-08) / 100 TABLET in 1 BOTTLE | Jan 13, 2022 |
| 25000-220-14 | 1000 TABLET in 1 BOTTLE (25000-220-14) | Jan 13, 2022 |
| 25000-220-78 | 1 BLISTER PACK in 1 CARTON (25000-220-78) / 7 TABLET in 1 BLISTER PACK | Apr 17, 2023 |
| 25000-220-81 | 1 BLISTER PACK in 1 CARTON (25000-220-81) / 14 TABLET in 1 BLISTER PACK | Jul 21, 2023 |