Metoclopramide Hydrochloride
- Product NDC
- 55154-6848
- 11-digit product format
- 551546848
- Labeler code
- 55154
- Product ID
- 55154-6848_71b04093-3d35-4b11-b6e6-334e6497076f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoclopramide Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA071250
- Marketing category
- ANDA
- Marketing start
- 2015-11-30
- 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
- 2020-12-31
- 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 |
|---|
| 55154-6848-0 | 55154684800 | 1 BLISTER PACK in 1 BAG (55154-6848-0) > 10 TABLET in 1 BLISTER PACK | 1 blister pack | 2015-11-30 | 0000-00-00 | No | No | Current |