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Primlev
Primlev - 59702-682-01 - (oxycodone and acetaminophen)
Drug Information of Primlev
| Product NDC: | 59702-682 |
| Proprietary Name: | Primlev |
| Non Proprietary Name: | oxycodone and acetaminophen |
| Active Ingredient(s): | 300; 7.5 mg/1; mg/1 & nbsp; oxycodone and acetaminophen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Primlev
| Product NDC: | 59702-682 |
| Labeler Name: | Atley Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040608 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100128 |
Package Information of Primlev
| Package NDC: | 59702-682-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (59702-682-01) |
NDC Information of Primlev
| NDC Code | 59702-682-01 |
| Proprietary Name | Primlev |
| Package Description | 100 TABLET in 1 BOTTLE (59702-682-01) |
| Product NDC | 59702-682 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | oxycodone and acetaminophen |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20100128 |
| Marketing Category Name | ANDA |
| Labeler Name | Atley Pharmaceuticals |
| Substance Name | ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE |
| Strength Number | 300; 7.5 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
