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PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN
PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN - 12634-537-82 - (PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN)
Drug Information of PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN
| Product NDC: | 12634-537 |
| 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, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN
| Product NDC: | 12634-537 |
| Labeler Name: | Apotheca, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074119 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090101 |
Package Information of PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN
| Package NDC: | 12634-537-82 |
| Package Description: | 12 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (12634-537-82) |
NDC Information of PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN
| NDC Code | 12634-537-82 |
| Proprietary Name | PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN |
| Package Description | 12 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (12634-537-82) |
| Product NDC | 12634-537 |
| 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 | 20090101 |
| Marketing Category Name | ANDA |
| Labeler Name | Apotheca, 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] |
