MECLIZINE HYDROCHLORIDE
- Product NDC
- 50090-2893
- 11-digit product format
- 500902893
- Labeler code
- 50090
- Product ID
- 50090-2893_f9b9b394-1d88-472b-9756-a173fdf07339
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Meclizine Hydrocloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- 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
- 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 |
|---|
| 50090-2893-0 | MECLIZINE HYDROCHLORIDE | 8 in 1 BOTTLE | TABLET | 8 | | 9 |
| 50090-2893-2 | MECLIZINE HYDROCHLORIDE | 12 in 1 BOTTLE | TABLET | 12 | | 9 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-2893 | MECLIZINE HYDROCHLORIDE (MECLIZINE HYDROCLORIDE) TABLET [A-S MEDICATION SOLUTIONS] | 9 | Legacy NDC, 2 package rows | 20211117_ea4a354b-05fe-47b4-9e96-bc7b5c4cadf2.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 |
|---|
| 50090-2893-0 | 50090289300 | 8 TABLET in 1 BOTTLE (50090-2893-0) | 8 tablet | 2017-03-01 | 0000-00-00 | No | No | Current |
| 50090-2893-2 | 50090289302 | 12 TABLET in 1 BOTTLE (50090-2893-2) | 12 tablet | 2019-10-29 | 0000-00-00 | No | No | Current |