NDC 48433-017 – Cetirizine Hydrochloride
Cetirizine Hydrochloride 10 mg/1 · Tablet, Film Coated · Oral
Product NDC48433-017
Product details
- Brand name
- Cetirizine Hydrochloride
- Generic name
- Cetirizine hydrochloride
- Labeler
- Safecor Health, LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA076677
- Marketed since
- April 17, 2026
- 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 (1)
| Package NDC | Description | Since |
|---|---|---|
| 48433-017-20 | 100 BLISTER PACK in 1 CARTON (48433-017-20) / 1 TABLET, FILM COATED in 1 BLISTER PACK (48433-017-01) | Apr 17, 2026 |
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