Meclizine Hydrochloride
- Product NDC
- 70518-1402
- 11-digit product format
- 705181402
- Labeler code
- 70518
- Product ID
- 70518-1402_e41794bf-4bdf-22ce-e053-2995a90a58c2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Meclizine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA201451
- Marketing category
- ANDA
- Marketing start
- 2018-09-06
- Marketing end
- 0000-00-00
- Substance
- MECLIZINE HYDROCHLORIDE
- Active strength
- 13 mg/1
- Pharmacologic classes
- Antiemetic [EPC], Emesis Suppression [PE]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 70518-1402-0 | 70518140200 | 30 TABLET in 1 BOTTLE, PLASTIC (70518-1402-0) | 30 tablet | 2018-09-06 | 0000-00-00 | No | No | Current |
| 70518-1402-1 | 70518140201 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-1402-1) | 90 tablet | 2019-01-17 | 0000-00-00 | No | No | Current |