NDC 68788-4072 – Cetirizine hydrochloride
Cetirizine Hydrochloride 10 mg/1 · Tablet, Film Coated · Oral
Product NDC68788-4072
Product details
- Brand name
- Cetirizine hydrochloride
- Generic name
- Cetirizine Hydrochloride
- Labeler
- Preferred Pharmaceuticals Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078336
- Marketed since
- January 27, 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 (3)
| Package NDC | Description | Since |
|---|---|---|
| 68788-4072-3 | 1 BOTTLE in 1 CARTON (68788-4072-3) / 30 TABLET, FILM COATED in 1 BOTTLE | Jan 27, 2026 |
| 68788-4072-6 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-4072-6) | Jan 27, 2026 |
| 68788-4072-9 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-4072-9) | Jan 27, 2026 |
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