MECLIZINE HYDROCHLORIDE
- Product NDC
- 70934-238
- 11-digit product format
- 709340238
- Labeler code
- 70934
- Product ID
- 70934-238_adddb1f8-7658-6523-e053-2995a90a1593
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Meclizine Hydrocloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. dba Northwind Pharmaceuticals
- Application
- ANDA040659
- Marketing category
- ANDA
- Marketing start
- 2019-01-09
- 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
- 2021-12-31
- 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 |
|---|
| 70934-238-08 | 70934023808 | 8 TABLET in 1 BOTTLE, PLASTIC (70934-238-08) | 8 tablet | 2019-10-30 | 0000-00-00 | No | No | Current |
| 70934-238-20 | 70934023820 | 20 TABLET in 1 BOTTLE, PLASTIC (70934-238-20) | 20 tablet | 2020-03-10 | 0000-00-00 | No | No | Current |
| 70934-238-30 | 70934023830 | 30 TABLET in 1 BOTTLE, PLASTIC (70934-238-30) | 30 tablet | 2019-01-09 | 0000-00-00 | No | No | Current |