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Propoxyphene Napsylate and Acetaminophen
Propoxyphene Napsylate and Acetaminophen - 49349-159-02 - (Propoxyphene Napsylate and Acetaminophen)
Drug Information of Propoxyphene Napsylate and Acetaminophen
| Product NDC: | 49349-159 |
| Proprietary Name: | Propoxyphene Napsylate and Acetaminophen |
| Non Proprietary Name: | Propoxyphene Napsylate and Acetaminophen |
| Active Ingredient(s): | 650; 100 mg/1; mg/1 & nbsp; Propoxyphene Napsylate and Acetaminophen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Propoxyphene Napsylate and Acetaminophen
| Product NDC: | 49349-159 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075738 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110215 |
Package Information of Propoxyphene Napsylate and Acetaminophen
| Package NDC: | 49349-159-02 |
| Package Description: | 30 TABLET in 1 BLISTER PACK (49349-159-02) |
NDC Information of Propoxyphene Napsylate and Acetaminophen
| NDC Code | 49349-159-02 |
| Proprietary Name | Propoxyphene Napsylate and Acetaminophen |
| Package Description | 30 TABLET in 1 BLISTER PACK (49349-159-02) |
| Product NDC | 49349-159 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Propoxyphene Napsylate and Acetaminophen |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20110215 |
| Marketing Category Name | ANDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE |
| Strength Number | 650; 100 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
