Oxycodone and Acetaminophen - Oxycodone hydrochloride and Acetaminophen
Navigation: NDC > Supplier starting with: W > WATSON LABORATORIES, INC.| Field | Value |
|---|---|
| NDC Code: | 0591-0824 |
| Proprietary Name: | Oxycodone and Acetaminophen |
| Suffix: | |
| Non-Proprietary Name: | Oxycodone hydrochloride and Acetaminophen |
| Dosage Form: | TABLET |
| Method: | ORAL |
| Original Marketing Date: | 29-12-2000 |
| Category Name: | ANDA |
| Application Number: | ANDA040371 |
| Labeler: | WATSON LABORATORIES, INC. |
| Substance Name: | ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE |
| Active Numerator Strength: | 500; 7.5 |
| Active Ingredient Unit: | mg/1; mg/1 |
| Pharm Classes: | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
| DEA Schedule: | CII |