Meclizine Hydrochloride
- Product NDC
- 70934-138
- 11-digit product format
- 709340138
- Labeler code
- 70934
- Product ID
- 70934-138_b930747a-b228-b587-e053-2a95a90a8eb4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Meclizine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA201451
- Marketing category
- ANDA
- Marketing start
- 2018-06-20
- 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 |
|---|
| 70934-138-30 | 70934013830 | 30 TABLET in 1 BOTTLE, PLASTIC (70934-138-30) | 30 tablet | 2018-06-20 | 0000-00-00 | No | No | Current |