Metoclopramide
- Product NDC
- 52584-414
- 11-digit product format
- 525840414
- Labeler code
- 52584
- Product ID
- 52584-414_4eeef8f6-93c2-4659-a238-34827b076b97
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoclopramide Hydrochloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- General Injectables & Vaccines, Inc.
- Application
- ANDA073118
- Marketing category
- ANDA
- Marketing start
- 2010-05-01
- Marketing end
- 2023-05-01
- Substance
- METOCLOPRAMIDE HYDROCHLORIDE
- Active strength
- 5 mg/mL
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 52584-414-01 | 52584041401 | 1 VIAL, SINGLE-DOSE in 1 BAG (52584-414-01) > 2 mL in 1 VIAL, SINGLE-DOSE | 2016-09-13 | 0000-00-00 | No | No | Current |