Metoclopramide Hydrochloride
- Product NDC
- 66689-031
- 11-digit product format
- 666890031
- Labeler code
- 66689
- Product ID
- 66689-031_d878f7b4-d7b5-4db0-9e97-dde119731159
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoclopramide Hydrochloride
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- VistaPharm, LLC
- Application
- ANDA075051
- Marketing category
- ANDA
- Marketing start
- 2010-02-12
- Marketing end
- 0000-00-00
- Substance
- METOCLOPRAMIDE HYDROCHLORIDE
- Active strength
- 5 mg/5mL
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 66689-031-50 | 66689003150 | 5 TRAY in 1 CASE (66689-031-50) > 10 CUP, UNIT-DOSE in 1 TRAY > 10 mL in 1 CUP, UNIT-DOSE (66689-031-01) | 5 tray | 2010-02-12 | 0000-00-00 | No | No | Current |