MECLIZINE HYDROCHLORIDE
- Product NDC
- 67296-1041
- 11-digit product format
- 672961041
- Labeler code
- 67296
- Product ID
- 67296-1041_d60f91b5-2530-145d-e053-2995a90af686
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- MECLIZINE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- ANDA040659
- Marketing category
- ANDA
- Marketing start
- 2010-06-04
- 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
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 67296-1041-1 | MECLIZINE HYDROCHLORIDE | 15 in 1 BOTTLE | TABLET | 15 | | 8 |
| 67296-1041-3 | MECLIZINE HYDROCHLORIDE | 30 in 1 BOTTLE | TABLET | 30 | | 8 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-1041 | MECLIZINE HYDROCHLORIDE TABLET [REDPHARM DRUG, INC.] | 8 | Legacy NDC, 2 package rows | 20240712_4e3ca2b3-8e1e-439f-e054-00144ff88e88.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 67296-1041-1 | 67296104101 | 15 TABLET in 1 BOTTLE (67296-1041-1) | 15 tablet | 2010-06-04 | 0000-00-00 | No | No | Current |
| 67296-1041-3 | 67296104103 | 30 TABLET in 1 BOTTLE (67296-1041-3) | 30 tablet | 2010-06-04 | 0000-00-00 | No | No | Current |