Meclizine Hydrochloride
- Product NDC
- 67296-1809
- 11-digit product format
- 672961809
- Labeler code
- 67296
- Product ID
- 67296-1809_d61f1e61-edf4-fddb-e053-2995a90ad1df
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Meclizine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- ANDA201451
- Marketing category
- ANDA
- Marketing start
- 2010-02-12
- 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 |
|---|
| 67296-1809-3 | Meclizine Hydrochloride | 30 in 1 BOTTLE | TABLET | 30 | | 6 |
| 67296-1809-7 | Meclizine Hydrochloride | 21 in 1 BOTTLE | TABLET | 21 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-1809 | MECLIZINE HYDROCHLORIDE TABLET [REDPHARM DRUG, INC.] | 6 | Legacy NDC, 2 package rows | 20240727_afedd989-3579-a973-e053-2995a90a6975.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 |
|---|
| 67296-1809-3 | 67296180903 | 30 TABLET in 1 BOTTLE (67296-1809-3) | 30 tablet | 2010-02-12 | 0000-00-00 | No | No | Current |
| 67296-1809-7 | 67296180907 | 21 TABLET in 1 BOTTLE (67296-1809-7) | 21 tablet | 2010-02-12 | 0000-00-00 | No | No | Current |