Naltrexone Hydrochloride
- Product NDC
- 50090-4926
- 11-digit product format
- 500904926
- Labeler code
- 50090
- Product ID
- 50090-4926_2ce79c32-5c7a-444f-b748-885202e5ccce
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Naltrexone Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA091205
- Marketing category
- ANDA
- Marketing start
- 2012-01-18
- 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
- 2023-12-31
- 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 |
|---|
| 50090-4926-0 | 50090492600 | 30 BLISTER PACK in 1 BOX, UNIT-DOSE (50090-4926-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK | 30 blister pack | 2022-11-02 | 0000-00-00 | No | No | Current |