NDC 71335-0789 – Levocetirizine Dihydrochloride
Levocetirizine Dihydrochloride 5 mg/1 · Tablet · Oral
Product NDC71335-0789
Product details
- Brand name
- Levocetirizine Dihydrochloride
- Generic name
- Levocetirizine Dihydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA091264
- Marketed since
- June 29, 2012
- 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 |
|---|---|---|
| 71335-0789-1 | 30 TABLET in 1 BOTTLE (71335-0789-1) | Jan 11, 2019 |
| 71335-0789-2 | 90 TABLET in 1 BOTTLE (71335-0789-2) | May 17, 2018 |
| 71335-0789-3 | 28 TABLET in 1 BOTTLE (71335-0789-3) | Dec 27, 2021 |
| 71335-0789-4 | 60 TABLET in 1 BOTTLE (71335-0789-4) | Dec 27, 2021 |
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