NALTREXONE HYDROCHLORIDE - NALTREXONE HYDROCHLORIDE
Navigation: NDC > Supplier starting with: S > SUN PHARMA GLOBAL FZE| Field | Value |
|---|---|
| NDC Code: | 47335-326 |
| Proprietary Name: | NALTREXONE HYDROCHLORIDE |
| Suffix: | |
| Non-Proprietary Name: | NALTREXONE HYDROCHLORIDE |
| Dosage Form: | TABLET, FILM COATED |
| Method: | ORAL |
| Original Marketing Date: | 29-02-2012 |
| Category Name: | ANDA |
| Application Number: | ANDA090356 |
| Labeler: | SUN PHARMA GLOBAL FZE |
| Substance Name: | NALTREXONE HYDROCHLORIDE |
| Active Numerator Strength: | 50 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | Opioid Antagonist [EPC],Opioid Antagonists [MoA] |
| DEA Schedule: |