Home
>
National Drug Code (NDC)
>
Primlev
Primlev - 24090-681-85 - (oxycodone and acetaminophen)
Drug Information of Primlev
| Product NDC: | 24090-681 |
| Proprietary Name: | Primlev |
| Non Proprietary Name: | oxycodone and acetaminophen |
| Active Ingredient(s): | 300; 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: | 24090-681 |
| Labeler Name: | Akrimax Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040608 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20111201 |
Package Information of Primlev
| Package NDC: | 24090-681-85 |
| Package Description: | 30 TABLET in 1 BOTTLE, PLASTIC (24090-681-85) |
NDC Information of Primlev
| NDC Code | 24090-681-85 |
| Proprietary Name | Primlev |
| Package Description | 30 TABLET in 1 BOTTLE, PLASTIC (24090-681-85) |
| Product NDC | 24090-681 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | oxycodone and acetaminophen |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20111201 |
| Marketing Category Name | ANDA |
| Labeler Name | Akrimax Pharmaceuticals, LLC |
| Substance Name | ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE |
| Strength Number | 300; 5 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
