Metoclopramide
- Product NDC
- 55154-8196
- 11-digit product format
- 551548196
- Labeler code
- 55154
- Product ID
- 55154-8196_5006cabb-ee65-4853-9113-0a132d9e26d8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoclopramide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Cardinal Health 107, LLC
- 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 |
|---|
| 55154-8196-0 | 55154819600 | 10 BLISTER PACK in 1 BAG (55154-8196-0) > 1 TABLET in 1 BLISTER PACK | 10 blister pack | 2015-11-30 | 2023-06-30 | No | No | Current |