Metoclopramide
- Product NDC
- 63629-7967
- 11-digit product format
- 636297967
- Labeler code
- 63629
- Product ID
- 63629-7967_15b1706b-bcb3-4308-8916-0fb1868de0af
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoclopramide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA070581
- Marketing category
- ANDA
- Marketing start
- 1985-10-17
- Marketing end
- 2023-10-31
- Substance
- METOCLOPRAMIDE HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Dopamine D2 Antagonists [MoA], Dopamine-2 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-7967-1 | 63629796701 | 20 TABLET in 1 BOTTLE (63629-7967-1) | 20 tablet | 2019-03-13 | 2023-10-31 | No | No | Current |