Naltrexone Hydrochloride - Naltrexone Hydrochloride
Navigation: NDC > Supplier starting with: P > PD RX PHARMACEUTICALS, INC.| Field | Value |
|---|---|
| NDC Code: | 43063-469 |
| Proprietary Name: | Naltrexone Hydrochloride |
| Suffix: | |
| Non-Proprietary Name: | Naltrexone Hydrochloride |
| Dosage Form: | TABLET, FILM COATED |
| Method: | ORAL |
| Original Marketing Date: | 08-05-1998 |
| Category Name: | ANDA |
| Application Number: | ANDA074918 |
| Labeler: | PD RX PHARMACEUTICALS, INC. |
| Substance Name: | NALTREXONE HYDROCHLORIDE |
| Active Numerator Strength: | 50 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | Opioid Antagonist [EPC],Opioid Antagonists [MoA] |
| DEA Schedule: |