Meclizine Hydrochloride
- Product NDC
- 50090-0107
- 11-digit product format
- 500900107
- Labeler code
- 50090
- Product ID
- 50090-0107_c62d34e1-5eab-41b6-930a-3fda8a165a3b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Meclizine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- 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
- 2021-12-31
- 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 |
|---|
| 50090-0107-2 | 50090010702 | 12 TABLET in 1 BOTTLE (50090-0107-2) | 12 tablet | 2018-04-06 | 0000-00-00 | No | No | Current |