Metoclopramide
- Product NDC
- 49999-057
- 11-digit product format
- 499990057
- Labeler code
- 49999
- Product ID
- 49999-057_8d051ff2-bb22-458c-bee2-b9ab86af240c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoclopramide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Quality Care Products LLC
- Application
- ANDA070184
- Marketing category
- ANDA
- Marketing start
- 1990-09-30
- Marketing end
- 0000-00-00
- 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
- 2023-12-31
- 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 |
|---|
| 49999-057-30 | 49999005730 | 30 TABLET in 1 BOTTLE (49999-057-30) | 30 tablet | 2013-09-10 | 0000-00-00 | No | No | Current |
| 49999-057-90 | 49999005790 | 90 TABLET in 1 BOTTLE (49999-057-90) | 90 tablet | 2016-03-11 | 0000-00-00 | No | No | Current |