Metoclopramide
- Product NDC
- 63629-6397
- 11-digit product format
- 636296397
- Labeler code
- 63629
- Product ID
- 63629-6397_2b956ad5-1167-46ef-8a1a-5c11e227f5ca
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoclopramide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA070184
- Marketing category
- ANDA
- Marketing start
- 1990-09-30
- 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
- 2021-12-31
- 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 |
|---|
| 63629-6397-1 | 63629639701 | 120 TABLET in 1 BOTTLE (63629-6397-1) | 120 tablet | 2015-09-17 | 0000-00-00 | No | No | Current |