Metoclopramide
- Product NDC
- 68071-4326
- 11-digit product format
- 680714326
- Labeler code
- 68071
- Product ID
- 68071-4326_bcab21cc-89ed-0de5-e053-2a95a90af8d0
- 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 |
|---|
| 68071-4326-2 | 68071432602 | 20 TABLET in 1 BOTTLE (68071-4326-2) | 20 tablet | 2018-03-12 | 0000-00-00 | No | No | Current |
| 68071-4326-3 | 68071432603 | 30 TABLET in 1 BOTTLE (68071-4326-3) | 30 tablet | 2018-03-12 | 0000-00-00 | No | No | Current |
| 68071-4326-9 | 68071432609 | 90 TABLET in 1 BOTTLE (68071-4326-9) | 90 tablet | 2018-03-12 | 0000-00-00 | No | No | Current |