Meclizine Hydrochloride
- Product NDC
- 60760-425
- 11-digit product format
- 607600425
- Labeler code
- 60760
- Product ID
- 60760-425_7abbcbbf-be68-3aac-e053-2991aa0a201b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Meclizine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA200294
- Marketing category
- ANDA
- Marketing start
- 2012-04-30
- 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
- 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 |
|---|
| 60760-425-30 | 60760042530 | 30 TABLET in 1 BOTTLE, PLASTIC (60760-425-30) | 30 tablet | 2017-12-14 | 0000-00-00 | No | No | Current |
| 60760-425-90 | 60760042590 | 90 TABLET in 1 BOTTLE, PLASTIC (60760-425-90) | 90 tablet | 2017-12-14 | 0000-00-00 | No | No | Current |