Naloxone Hydrochloride - Naloxone Hydrochloride
Navigation: NDC > Supplier starting with: A > AMPHASTAR PHARMACEUTICALS, INC.| Field | Value |
|---|---|
| NDC Code: | 0548-3369 |
| Proprietary Name: | Naloxone Hydrochloride |
| Suffix: | |
| Non-Proprietary Name: | Naloxone Hydrochloride |
| Dosage Form: | INJECTION |
| Method: | PARENTERAL |
| Original Marketing Date: | 01-06-2001 |
| Category Name: | ANDA |
| Application Number: | ANDA072076 |
| Labeler: | AMPHASTAR PHARMACEUTICALS, INC. |
| Substance Name: | NALOXONE HYDROCHLORIDE |
| Active Numerator Strength: | 1 |
| Active Ingredient Unit: | mg/mL |
| Pharm Classes: | Opioid Antagonist [EPC],Opioid Antagonists [MoA] |
| DEA Schedule: |