Metoclopramide
- Product NDC
- 76045-213
- 11-digit product format
- 760450213
- Labeler code
- 76045
- Product ID
- 76045-213_4a411ded-d608-41d3-bb26-67d5d5d3c9b5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoclopramide Hydrochloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Fresenius Kabi USA, LLC
- Application
- ANDA091392
- Marketing category
- ANDA
- Marketing start
- 2013-05-03
- Substance
- METOCLOPRAMIDE HYDROCHLORIDE
- Active strength
- 10 mg/2mL
- Pharmacologic classes
- Dopamine D2 Antagonists [MoA], Dopamine-2 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| W1792A2RVD | METOCLOPRAMIDE HYDROCHLORIDE | 54143-57-6 | METOCLOPRAMIDE HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 76045-213-20 | 76045021320 | 24 BLISTER PACK in 1 CARTON (76045-213-20) / 1 SYRINGE, GLASS in 1 BLISTER PACK (76045-213-00) / 2 mL in 1 SYRINGE, GLASS | 24 blister pack | 2022-02-28 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Metoclopramide Injection, USP | Fresenius Kabi USA, LLC | Fresenius Kabi, USA LLC | 2023-06-07 | HUMAN PRESCRIPTION DRUG LABEL | 12 |