Meclizine Hydrochloride
- Product NDC
- 70518-2304
- 11-digit product format
- 705182304
- Labeler code
- 70518
- Product ID
- 70518-2304_ea4aff76-2a31-3f13-e053-2995a90a51db
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Meclizine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA201451
- Marketing category
- ANDA
- Marketing start
- 2019-09-09
- 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
- 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 |
|---|
| 70518-2304-0 | 70518230400 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-2304-0) | 90 tablet | 2019-09-09 | 0000-00-00 | No | No | Current |
| 70518-2304-1 | 70518230401 | 60 TABLET in 1 BOTTLE, PLASTIC (70518-2304-1) | 60 tablet | 2019-10-04 | 0000-00-00 | No | No | Current |
| 70518-2304-2 | 70518230402 | 30 TABLET in 1 BOTTLE, PLASTIC (70518-2304-2) | 30 tablet | 2020-02-11 | 0000-00-00 | No | No | Current |
| 70518-2304-3 | 70518230403 | 30 TABLET in 1 BOTTLE, PLASTIC (70518-2304-3) | 30 tablet | 2021-06-08 | 0000-00-00 | No | No | Current |