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Propoxyphene and Acetaminophen
Propoxyphene and Acetaminophen - 63874-201-90 - (propoxyphene napsylate and acetaminophen)
Drug Information of Propoxyphene and Acetaminophen
| Product NDC: | 63874-201 |
| Proprietary Name: | Propoxyphene 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, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Propoxyphene and Acetaminophen
| Product NDC: | 63874-201 |
| Labeler Name: | Altura Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074843 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100101 |
Package Information of Propoxyphene and Acetaminophen
| Package NDC: | 63874-201-90 |
| Package Description: | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63874-201-90) |
NDC Information of Propoxyphene and Acetaminophen
| NDC Code | 63874-201-90 |
| Proprietary Name | Propoxyphene and Acetaminophen |
| Package Description | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63874-201-90) |
| Product NDC | 63874-201 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | propoxyphene napsylate and acetaminophen |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20100101 |
| Marketing Category Name | ANDA |
| Labeler Name | Altura Pharmaceuticals, 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] |
