NDC 0093-7701 – Levocetirizine Dihydrochloride
Levocetirizine Dihydrochloride 5 mg/1 · Tablet, Film Coated · Oral
Product NDC0093-7701
Product details
- Brand name
- Levocetirizine Dihydrochloride
- Generic name
- Levocetirizine Dihydrochloride
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA090199
- Marketed since
- September 6, 2011
- 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 (1)
| Package NDC | Description | Since |
|---|---|---|
| 0093-7701-98 | 90 TABLET, FILM COATED in 1 BOTTLE (0093-7701-98) | Sep 6, 2011 |
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