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Propoxyphene
Propoxyphene - 55289-834-20 - (Propoxyphene Hydrochloride)
Drug Information of Propoxyphene
| Product NDC: | 55289-834 |
| Proprietary Name: | Propoxyphene |
| Non Proprietary Name: | Propoxyphene Hydrochloride |
| Active Ingredient(s): | 65 mg/1 & nbsp; Propoxyphene Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Propoxyphene
| Product NDC: | 55289-834 |
| Labeler Name: | PD-Rx Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA083501 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100510 |
Package Information of Propoxyphene
| Package NDC: | 55289-834-20 |
| Package Description: | 20 CAPSULE in 1 BOTTLE, PLASTIC (55289-834-20) |
NDC Information of Propoxyphene
| NDC Code | 55289-834-20 |
| Proprietary Name | Propoxyphene |
| Package Description | 20 CAPSULE in 1 BOTTLE, PLASTIC (55289-834-20) |
| Product NDC | 55289-834 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Propoxyphene Hydrochloride |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20100510 |
| Marketing Category Name | ANDA |
| Labeler Name | PD-Rx Pharmaceuticals, Inc. |
| Substance Name | PROPOXYPHENE HYDROCHLORIDE |
| Strength Number | 65 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
