Metoclopramide
- Product NDC
- 71335-0790
- 11-digit product format
- 713350790
- Labeler code
- 71335
- Product ID
- 71335-0790_2e5ed77b-8d8c-4a8e-93a9-ca524e543e2e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoclopramide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA070581
- Marketing category
- ANDA
- Marketing start
- 1985-10-17
- Marketing end
- 2023-10-31
- 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 |
|---|
| 71335-0790-1 | 71335079001 | 30 TABLET in 1 BOTTLE (71335-0790-1) | 30 tablet | 2018-04-23 | 2023-10-31 | No | No | Current |
| 71335-0790-2 | 71335079002 | 90 TABLET in 1 BOTTLE (71335-0790-2) | 90 tablet | 2019-02-14 | 2023-10-31 | No | No | Current |
| 71335-0790-3 | 71335079003 | 60 TABLET in 1 BOTTLE (71335-0790-3) | 60 tablet | 2021-12-27 | 2023-10-31 | No | No | Current |
| 71335-0790-4 | 71335079004 | 10 TABLET in 1 BOTTLE (71335-0790-4) | 10 tablet | 2021-12-27 | 2023-10-31 | No | No | Current |
| 71335-0790-5 | 71335079005 | 20 TABLET in 1 BOTTLE (71335-0790-5) | 20 tablet | 2020-06-25 | 2023-10-31 | No | No | Current |
| 71335-0790-6 | 71335079006 | 100 TABLET in 1 BOTTLE (71335-0790-6) | 100 tablet | 2021-12-27 | 2023-10-31 | No | No | Current |