Meclizine Hydrochloride
- Product NDC
- 50090-5727
- 11-digit product format
- 500905727
- Labeler code
- 50090
- Product ID
- 50090-5727_9d0bedaa-8707-4659-b79d-f34989c2d26c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Meclizine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA213957
- Marketing category
- ANDA
- Marketing start
- 2020-10-29
- Substance
- MECLIZINE HYDROCHLORIDE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Antiemetic [EPC], Emesis Suppression [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| HDP7W44CIO | MECLIZINE HYDROCHLORIDE | 31884-77-2 | MECLIZINE HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-5727-2 | 50090572702 | 12 TABLET in 1 BOTTLE (50090-5727-2) | 12 tablet | 2021-09-28 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Meclizine Hydrochloride | A-S Medication Solutions | 2023-04-19 | HUMAN PRESCRIPTION DRUG LABEL | 1 |