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Propoxyphene Hydrochloride and Acetaminophen
Propoxyphene Hydrochloride and Acetaminophen - 0378-0130-05 - (propoxyphene hydrochloride and acetaminophen)
Drug Information of Propoxyphene Hydrochloride and Acetaminophen
| Product NDC: | 0378-0130 |
| Proprietary Name: | Propoxyphene Hydrochloride and Acetaminophen |
| Non Proprietary Name: | propoxyphene hydrochloride and acetaminophen |
| Active Ingredient(s): | 650; 65 mg/1; mg/1 & nbsp; propoxyphene hydrochloride and acetaminophen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Propoxyphene Hydrochloride and Acetaminophen
| Product NDC: | 0378-0130 |
| Labeler Name: | Mylan Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA083978 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091130 |
Package Information of Propoxyphene Hydrochloride and Acetaminophen
| Package NDC: | 0378-0130-05 |
| Package Description: | 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0130-05) |
NDC Information of Propoxyphene Hydrochloride and Acetaminophen
| NDC Code | 0378-0130-05 |
| Proprietary Name | Propoxyphene Hydrochloride and Acetaminophen |
| Package Description | 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0130-05) |
| Product NDC | 0378-0130 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | propoxyphene hydrochloride and acetaminophen |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20091130 |
| Marketing Category Name | ANDA |
| Labeler Name | Mylan Pharmaceuticals Inc. |
| Substance Name | ACETAMINOPHEN; PROPOXYPHENE HYDROCHLORIDE |
| Strength Number | 650; 65 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
