MECLIZINE HYDROCHLORIDE
- Product NDC
- 68071-3308
- 11-digit product format
- 680713308
- Labeler code
- 68071
- Product ID
- 68071-3308_bb2b3c0a-6723-4030-e053-2a95a90ac206
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Meclizine Hydrochloride
- 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
- 13 mg/1
- Pharmacologic classes
- Antiemetic [EPC],Emesis Suppression [PE]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-3308-2 | 68071330802 | 20 TABLET in 1 BOTTLE (68071-3308-2) | 20 tablet | 2018-01-17 | 0000-00-00 | No | No | Current |
| 68071-3308-3 | 68071330803 | 30 TABLET in 1 BOTTLE (68071-3308-3) | 30 tablet | 2018-01-17 | 0000-00-00 | No | No | Current |
| 68071-3308-6 | 68071330806 | 60 TABLET in 1 BOTTLE (68071-3308-6) | 60 tablet | 2018-01-17 | 0000-00-00 | No | No | Current |
| 68071-3308-9 | 68071330809 | 90 TABLET in 1 BOTTLE (68071-3308-9) | 90 tablet | 2018-01-17 | 0000-00-00 | No | No | Current |