MECLIZINE HYDROCHLORIDE
- Product NDC
- 63629-7965
- 11-digit product format
- 636297965
- Labeler code
- 63629
- Product ID
- 63629-7965_ffe71cc1-a11f-435b-a9c3-31bbaef7ed89
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Meclizine Hydrocloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- 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
- 2020-12-31
- 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 |
|---|
| 63629-7965-1 | 63629796501 | 20 TABLET in 1 BOTTLE (63629-7965-1) | 20 tablet | 2019-03-13 | 0000-00-00 | No | No | Current |