Meclizine hydrochloride
- Product NDC
- 52536-137
- 11-digit product format
- 525360137
- Labeler code
- 52536
- Product ID
- 52536-137_c00045b2-67b8-4f8a-a1de-f76137acfc3d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Meclizine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Wilshire Pharmaceuticals Inc
- Application
- ANDA205136
- Marketing category
- ANDA
- Marketing start
- 2019-04-15
- Marketing end
- 0000-00-00
- Substance
- MECLIZINE HYDROCHLORIDE
- Active strength
- 50 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 |
|---|
| 52536-137-01 | 52536013701 | 100 TABLET in 1 BOTTLE (52536-137-01) | 100 tablet | 2019-04-15 | 0000-00-00 | No | No | Current |
| 52536-137-10 | 52536013710 | 1000 TABLET in 1 BOTTLE (52536-137-10) | 1000 tablet | 2019-04-15 | 0000-00-00 | No | No | Current |