Meclizine Hydrochloride
- Product NDC
- 68071-4497
- 11-digit product format
- 680714497
- Labeler code
- 68071
- Product ID
- 68071-4497_bb8add3c-11f3-7096-e053-2995a90a323c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Meclizine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA201451
- Marketing category
- ANDA
- Marketing start
- 2010-02-12
- 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
- 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 |
|---|
| 68071-4497-6 | 68071449706 | 6 TABLET in 1 BOTTLE (68071-4497-6) | 6 tablet | 2018-07-17 | 0000-00-00 | No | No | Current |