MECLIZINE HYDROCHLORIDE
- Product NDC
- 68071-4694
- 11-digit product format
- 680714694
- Labeler code
- 68071
- Product ID
- 68071-4694_d58ecd75-209f-699e-e053-2a95a90a0730
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Meclizine Hydrocloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA040659
- Marketing category
- ANDA
- Marketing start
- 2010-06-04
- Marketing end
- 0000-00-00
- Substance
- MECLIZINE HYDROCHLORIDE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Antiemetic [EPC], Emesis Suppression [PE]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-4694-4 | 68071469404 | 4 TABLET in 1 BOTTLE (68071-4694-4) | 4 tablet | 2019-01-07 | 0000-00-00 | No | No | Current |
| 68071-4694-6 | 68071469406 | 60 TABLET in 1 BOTTLE (68071-4694-6) | 60 tablet | 2019-01-07 | 0000-00-00 | No | No | Current |