MECLIZINE HYDROCHLORIDE
- Product NDC
- 43063-899
- 11-digit product format
- 430630899
- Labeler code
- 43063
- Product ID
- 43063-899_dad00eee-92ca-7610-e053-2a95a90a1fac
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Meclizine Hydrocloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- 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
- 2023-12-31
- 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 |
|---|
| 43063-899-10 | 43063089910 | 10 TABLET in 1 BOTTLE, PLASTIC (43063-899-10) | 10 tablet | 2018-09-25 | 0000-00-00 | No | No | Current |
| 43063-899-15 | 43063089915 | 15 TABLET in 1 BOTTLE, PLASTIC (43063-899-15) | 15 tablet | 2018-09-25 | 0000-00-00 | No | No | Current |
| 43063-899-30 | 43063089930 | 30 TABLET in 1 BOTTLE, PLASTIC (43063-899-30) | 30 tablet | 2018-09-25 | 0000-00-00 | No | No | Current |