Meclizine Hydrochloride
- Product NDC
- 70771-1540
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Meclizine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Zydus Lifesciences Limited
- Application
- ANDA213957
- Marketing category
- ANDA
- Substance
- MECLIZINE HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 70771-1540-0 | 1000 TABLET in 1 BOTTLE (70771-1540-0) | 2020-10-29 | | No | Historical |
| 70771-1540-1 | 100 TABLET in 1 BOTTLE (70771-1540-1) | 2020-10-29 | | No | Historical |
| 70771-1540-3 | 30 TABLET in 1 BOTTLE (70771-1540-3) | 2020-10-29 | | No | Historical |
| 70771-1540-4 | 10 BLISTER PACK in 1 CARTON (70771-1540-4) / 10 TABLET in 1 BLISTER PACK (70771-1540-2) | 2020-10-29 | | No | Historical |
| 70771-1540-9 | 90 TABLET in 1 BOTTLE (70771-1540-9) | 2020-10-29 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Meclizine Hydrochloride | Zydus Lifesciences Limited | 2023-08-28 | HUMAN PRESCRIPTION DRUG LABEL | 2 |