MECLIZINE HYDROCHLORIDE
- Product NDC
- 71335-1563
- 11-digit product format
- 713351563
- Labeler code
- 71335
- Product ID
- 71335-1563_7e501fc0-081b-4e64-b2fd-e2193ddb55b6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Meclizine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA040659
- Marketing category
- ANDA
- Marketing start
- 2010-06-04
- Substance
- MECLIZINE HYDROCHLORIDE
- Active strength
- 12.5 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 |
|---|
| 71335-1563-1 | 71335156301 | 30 TABLET in 1 BOTTLE (71335-1563-1) | 30 tablet | 2010-06-04 | No | No | Historical |
| 71335-1563-2 | 71335156302 | 60 TABLET in 1 BOTTLE (71335-1563-2) | 60 tablet | 2010-06-04 | No | No | Historical |
| 71335-1563-3 | 71335156303 | 90 TABLET in 1 BOTTLE (71335-1563-3) | 90 tablet | 2010-06-04 | No | No | Historical |
| 71335-1563-4 | 71335156304 | 28 TABLET in 1 BOTTLE (71335-1563-4) | 28 tablet | 2010-06-04 | No | No | Historical |
| 71335-1563-5 | 71335156305 | 20 TABLET in 1 BOTTLE (71335-1563-5) | 20 tablet | 2010-06-04 | No | No | Historical |
| 71335-1563-6 | 71335156306 | 120 TABLET in 1 BOTTLE (71335-1563-6) | 120 tablet | 2010-06-04 | No | No | Historical |
| 71335-1563-7 | 71335156307 | 100 TABLET in 1 BOTTLE (71335-1563-7) | 100 tablet | 2010-06-04 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| MECLIZINE HYDROCHLORIDE | Bryant Ranch Prepack | 2020-05-22 | HUMAN PRESCRIPTION DRUG LABEL | 1 |