Naltrexone Hydrochloride
- Product NDC
- 68071-2156
- 11-digit product format
- 680712156
- Labeler code
- 68071
- Product ID
- 68071-2156_af86d6b3-98cb-528b-e053-2995a90a7da9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Naltrexone Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticls, Inc.
- Application
- ANDA075274
- Marketing category
- ANDA
- Marketing start
- 2013-09-23
- Marketing end
- 0000-00-00
- Substance
- NALTREXONE HYDROCHLORIDE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Opioid Antagonist [EPC],Opioid Antagonists [MoA]
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-2156-3 | 68071215603 | 30 TABLET, FILM COATED in 1 BOTTLE (68071-2156-3) | 2017-01-25 | 0000-00-00 | No | No | Current |