Metoclopramide
- Product NDC
- 68071-4569
- 11-digit product format
- 680714569
- Labeler code
- 68071
- Product ID
- 68071-4569_bbeff419-8524-5bd1-e053-2a95a90a2539
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoclopramide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA070581
- Marketing category
- ANDA
- Marketing start
- 1985-10-17
- Marketing end
- 0000-00-00
- 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
- 2022-12-31
- 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 |
|---|
| 68071-4569-6 | 68071456906 | 6 TABLET in 1 BOTTLE (68071-4569-6) | 6 tablet | 2018-09-20 | 0000-00-00 | No | No | Current |