Meclizine Hydrochloride
- Product NDC
- 76420-799
- 11-digit product format
- 764200799
- Labeler code
- 76420
- Product ID
- 76420-799_158f70ad-1608-c116-e063-6394a90a94c6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Meclizine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Asclemed USA, Inc.
- Application
- NDA010721
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2020-01-15
- Substance
- MECLIZINE HYDROCHLORIDE
- Active strength
- 50 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 |
|---|
| 76420-799-01 | 76420079901 | 100 TABLET in 1 BOTTLE (76420-799-01) | 100 tablet | 2024-04-05 | No | No | Historical |
| 76420-799-30 | 76420079930 | 30 TABLET in 1 BOTTLE (76420-799-30) | 30 tablet | 2024-04-05 | No | No | Historical |
| 76420-799-60 | 76420079960 | 60 TABLET in 1 BOTTLE (76420-799-60) | 60 tablet | 2024-04-05 | No | No | Historical |
| 76420-799-90 | 76420079990 | 90 TABLET in 1 BOTTLE (76420-799-90) | 90 tablet | 2024-04-05 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Meclizine Hydrochloride | Asclemed USA, Inc. | ASCLEMED USA INC. DBA ENOVACHEM | 2024-04-08 | HUMAN PRESCRIPTION DRUG LABEL | 1 |