Meclizine HCl 25 mg
- Product NDC
- 50436-0994
- 11-digit product format
- 504360994
- Labeler code
- 50436
- Product ID
- 50436-0994_402427ef-1da7-48c7-84d0-982e25cf0c8b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Meclizine Hydrochloride
- Dosage form
- TABLET, CHEWABLE
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- part336
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2015-10-15
- Marketing end
- 0000-00-00
- Substance
- MECLIZINE HYDROCHLORIDE
- Active strength
- 25 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 50436-0994-1 | Meclizine HCl 25 mg | 30 in 1 BOTTLE | TABLET, CHEWABLE | 30 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50436-0994 | MECLIZINE HCL 25 MG (MECLIZINE HYDROCHLORIDE) TABLET, CHEWABLE [UNIT DOSE SERVICES] | 4 | Legacy NDC, 1 package rows | 20210923_ff14ae8b-bc67-4f79-958a-c2d968bfcc30.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50436-0994-1 | 50436099401 | 30 TABLET, CHEWABLE in 1 BOTTLE (50436-0994-1) | 2017-12-05 | 0000-00-00 | No | No | Current |