Meclizine Hydrochloride
- Product NDC
- 0904-6517
- 11-digit product format
- 009046517
- Labeler code
- 0904
- Product ID
- 0904-6517_f7ceaf71-c39a-45fa-aa42-e77a707b11a5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Meclizine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- 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
- 2022-12-31
- 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 |
|---|
| 0904-6517-61 | 00904651761 | 100 BLISTER PACK in 1 CARTON (0904-6517-61) > 1 TABLET in 1 BLISTER PACK | 100 blister pack | 2010-02-12 | 0000-00-00 | No | No | Current |