Meclizine Hydrochloride
- Product NDC
- 55700-912
- 11-digit product format
- 557000912
- Labeler code
- 55700
- Product ID
- 55700-912_900d0679-71e9-453c-87e9-50a68dd630c3
- 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
- 2021-05-20
- 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
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 55700-912 | MECLIZINE HYDROCHLORIDE TABLET [QUALITY CARE PRODUCTS, LLC] | 3 | Legacy NDC | 20241220_9fdf1e06-4e38-4dc0-b236-7f724518e95b.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-912-30 | 55700091230 | 30 TABLET in 1 BOTTLE (55700-912-30) | 30 tablet | 2021-05-20 | 0000-00-00 | No | No | Current |