MECLIZINE HYDROCHLORIDE
- Product NDC
- 50090-4577
- 11-digit product format
- 500904577
- Labeler code
- 50090
- Product ID
- 50090-4577_7345346e-2e75-4217-88d8-5e23ff533496
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Meclizine Hydrocloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- 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
- 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 |
|---|
| 50090-4577-0 | 50090457700 | 20 TABLET in 1 BOTTLE (50090-4577-0) | 20 tablet | 2019-10-04 | 0000-00-00 | No | No | Current |
| 50090-4577-1 | 50090457701 | 30 TABLET in 1 BOTTLE (50090-4577-1) | 30 tablet | 2019-10-04 | 0000-00-00 | No | No | Current |
| 50090-4577-4 | 50090457704 | 10 TABLET in 1 BOTTLE (50090-4577-4) | 10 tablet | 2019-10-04 | 0000-00-00 | No | No | Current |
| 50090-4577-8 | 50090457708 | 90 TABLET in 1 BOTTLE (50090-4577-8) | 90 tablet | 2019-10-04 | 0000-00-00 | No | No | Current |