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NALTREXONE HYDROCHLORIDE
NALTREXONE HYDROCHLORIDE - 47335-326-18 - (NALTREXONE HYDROCHLORIDE)
Drug Information of NALTREXONE HYDROCHLORIDE
| Product NDC: | 47335-326 |
| Proprietary Name: | NALTREXONE HYDROCHLORIDE |
| Non Proprietary Name: | NALTREXONE HYDROCHLORIDE |
| Active Ingredient(s): | 50 mg/1 & nbsp; NALTREXONE HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of NALTREXONE HYDROCHLORIDE
| Product NDC: | 47335-326 |
| Labeler Name: | Sun Pharma Global FZE |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090356 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120229 |
Package Information of NALTREXONE HYDROCHLORIDE
| Package NDC: | 47335-326-18 |
| Package Description: | 1000 TABLET, FILM COATED in 1 BOTTLE (47335-326-18) |
NDC Information of NALTREXONE HYDROCHLORIDE
| NDC Code | 47335-326-18 |
| Proprietary Name | NALTREXONE HYDROCHLORIDE |
| Package Description | 1000 TABLET, FILM COATED in 1 BOTTLE (47335-326-18) |
| Product NDC | 47335-326 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | NALTREXONE HYDROCHLORIDE |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20120229 |
| Marketing Category Name | ANDA |
| Labeler Name | Sun Pharma Global FZE |
| Substance Name | NALTREXONE HYDROCHLORIDE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Opioid Antagonist [EPC],Opioid Antagonists [MoA] |
