Metoclopramide
- Product NDC
- 71872-7075
- 11-digit product format
- 718727075
- Labeler code
- 71872
- Product ID
- 71872-7075_9ce5ad2c-3abe-78ff-e053-2995a90a514d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoclopramide
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Medical Purchasing Solutions, LLC
- Application
- ANDA073135
- Marketing category
- ANDA
- Marketing start
- 1991-12-01
- Marketing end
- 0000-00-00
- 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
- 2021-12-31
- 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 |
|---|
| 71872-7075-1 | 71872707501 | 1 VIAL, SINGLE-USE in 1 BAG (71872-7075-1) > 2 mL in 1 VIAL, SINGLE-USE | 2018-05-24 | 0000-00-00 | No | No | Current |