Metoclopramide
- Product NDC
- 68084-676
- 11-digit product format
- 680840676
- Labeler code
- 68084
- Product ID
- 68084-676_d954391a-375a-23e4-e053-2995a90a6345
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoclopramide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA070581
- Marketing category
- ANDA
- Marketing start
- 2015-11-30
- Marketing end
- 2023-06-30
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68084-676-01 | 68084067601 | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-676-01) > 1 TABLET in 1 BLISTER PACK (68084-676-11) | 100 blister pack | 2015-11-30 | 0000-00-00 | No | No | Current |