MECLIZINE HYDROCHLORIDE
- Product NDC
- 61919-752
- 11-digit product format
- 619190752
- Labeler code
- 61919
- Product ID
- 61919-752_04ca583b-3540-4011-8817-352ea0dac42e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- MECLIZINE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- DirectRX
- Application
- ANDA200294
- Marketing category
- ANDA
- Marketing start
- 2015-01-01
- Marketing end
- 0000-00-00
- Substance
- MECLIZINE HYDROCHLORIDE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Antiemetic [EPC],Emesis Suppression [PE]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 61919-752-30 | MECLIZINE HYDROCHLORIDE | 30 in 1 BOTTLE | TABLET | 30 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61919-752 | MECLIZINE HYDROCHLORIDE TABLET [DIRECTRX] | 1 | Legacy NDC, 1 package rows | 20151029_c66d4869-630e-4b9f-acfb-9fdd4d06d7de.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 61919-752-30 | 61919075230 | 30 in 1 BOTTLE | Historical |