Metoclopramide Hydrochloride
- Product NDC
- 68071-3262
- 11-digit product format
- 680713262
- Labeler code
- 68071
- Product ID
- 68071-3262_bb14e613-6640-b8b0-e053-2995a90a56de
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoclopramide Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA071250
- Marketing category
- ANDA
- Marketing start
- 2011-08-22
- 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
- 2022-12-31
- 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 |
|---|
| 68071-3262-2 | 68071326202 | 20 TABLET in 1 BOTTLE (68071-3262-2) | 20 tablet | 2017-06-08 | 0000-00-00 | No | No | Current |
| 68071-3262-3 | 68071326203 | 30 TABLET in 1 BOTTLE (68071-3262-3) | 30 tablet | 2017-06-08 | 0000-00-00 | No | No | Current |
| 68071-3262-6 | 68071326206 | 60 TABLET in 1 BOTTLE (68071-3262-6) | 60 tablet | 2017-06-08 | 0000-00-00 | No | No | Current |
| 68071-3262-9 | 68071326209 | 90 TABLET in 1 BOTTLE (68071-3262-9) | 90 tablet | 2017-06-08 | 0000-00-00 | No | No | Current |