NDC 70677-1007 – Cetirizine hydrochloride
Cetirizine Hydrochloride 10 mg/1 · Tablet, Film Coated · Oral
Product NDC70677-1007
Product details
- Brand name
- Cetirizine hydrochloride
- Generic name
- Cetirizine Hydrochloride Tablets
- Labeler
- Strategic Sourcing Services LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078343
- Marketed since
- May 12, 2022
- Marketing end
- February 28, 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 |
|---|---|---|
| 70677-1007-2 | 1 BOTTLE in 1 CARTON (70677-1007-2) / 60 TABLET, FILM COATED in 1 BOTTLE | May 5, 2023 |
| 70677-1007-3 | 1 BOTTLE in 1 CARTON (70677-1007-3) / 90 TABLET, FILM COATED in 1 BOTTLE | May 5, 2023 |
| 70677-1007-4 | 1 BOTTLE in 1 CARTON (70677-1007-4) / 300 TABLET, FILM COATED in 1 BOTTLE | May 5, 2023 |
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