Meclizine Hydrochloride
- Product NDC
- 55700-919
- 11-digit product format
- 557000919
- Labeler code
- 55700
- Product ID
- 55700-919_5ef91c7f-356c-4caf-be9d-8620b425e4d1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Meclizine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- NDA010721
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2021-07-29
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-919-30 | 55700091930 | 30 TABLET in 1 BOTTLE (55700-919-30) | 30 tablet | 2021-07-29 | 0000-00-00 | No | No | Current |