Meclizine Hydrochloride
- Product NDC
- 74074-003
- 11-digit product format
- 740740003
- Labeler code
- 74074
- Product ID
- 74074-003_bce6ddf3-867c-44f9-82c3-6c52b597d262
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Meclizine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Nortic Pharma, LLC
- Application
- NDA010721
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2020-10-15
- Marketing end
- 0000-00-00
- Substance
- MECLIZINE HYDROCHLORIDE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Antiemetic [EPC],Emesis Suppression [PE]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 74074-003-01 | 74074000301 | 100 TABLET in 1 BOTTLE (74074-003-01) | 100 tablet | 2020-10-15 | 0000-00-00 | No | No | Current |
| 74074-003-99 | 74074000399 | 1000 TABLET in 1 BOTTLE (74074-003-99) | 1000 tablet | 2020-10-15 | 0000-00-00 | No | No | Current |