NDC 68788-8810 – Levocetirizine Dihydrochloride
Levocetirizine Dihydrochloride 5 mg/1 · Tablet, Film Coated · Oral
Product NDC68788-8810
Product details
- Brand name
- Levocetirizine Dihydrochloride
- Generic name
- Levocetirizine Dihydrochloride
- Labeler
- Preferred Pharmaceuticals Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA205564
- Marketed since
- January 20, 2025
- Listing expires
- December 31, 2026
- Pharmacologic class
- Histamine-1 Receptor Antagonist
Active ingredients
Uses, dosage, side effects and warnings for Levocetirizine dihydrochloride →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 68788-8810-1 | 100 TABLET, FILM COATED in 1 BOTTLE (68788-8810-1) | Jan 20, 2025 |
| 68788-8810-3 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-8810-3) | Jan 20, 2025 |
| 68788-8810-6 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-8810-6) | Jan 20, 2025 |
| 68788-8810-9 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-8810-9) | Jan 20, 2025 |
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