NDC 55289-995 – Cetirizine Hydrochloride
Cetirizine Hydrochloride 10 mg/1 · Tablet · Oral
Product NDC55289-995
Product details
- Brand name
- Cetirizine Hydrochloride
- Generic name
- Cetirizine Hydrochloride
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA077498
- Marketed since
- December 27, 2007
- 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 (3)
| Package NDC | Description | Since |
|---|---|---|
| 55289-995-07 | 7 TABLET in 1 BOTTLE, PLASTIC (55289-995-07) | Mar 8, 2022 |
| 55289-995-10 | 10 TABLET in 1 BOTTLE, PLASTIC (55289-995-10) | Aug 9, 2022 |
| 55289-995-30 | 30 TABLET in 1 BOTTLE, PLASTIC (55289-995-30) | Apr 26, 2018 |
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