Metoclopramide Hydrochloride
- Product NDC
- 0115-1651
- 11-digit product format
- 001151651
- Labeler code
- 0115
- Product ID
- 0115-1651_b034eaab-fc17-4783-9561-f6a05056855c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoclopramide Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Amneal Pharmaceuticals of New York LLC
- Application
- ANDA071250
- Marketing category
- ANDA
- Marketing start
- 2011-08-22
- Marketing end
- 2021-10-31
- 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 |
|---|
| 0115-1651-01 | 00115165101 | 100 TABLET in 1 BOTTLE, PLASTIC (0115-1651-01) | 100 tablet | 2011-08-22 | 2021-03-31 | No | No | Current |
| 0115-1651-02 | 00115165102 | 500 TABLET in 1 BOTTLE, PLASTIC (0115-1651-02) | 500 tablet | 2011-08-22 | 2021-05-31 | No | No | Current |
| 0115-1651-03 | 00115165103 | 1000 TABLET in 1 BOTTLE, PLASTIC (0115-1651-03) | 1000 tablet | 2011-08-22 | 2021-10-31 | No | No | Current |