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Propoxyphene Hydrochloride
Propoxyphene Hydrochloride - 0378-7065-01 - (Propoxyphene Hydrochloride)
Drug Information of Propoxyphene Hydrochloride
| Product NDC: | 0378-7065 |
| Proprietary Name: | Propoxyphene Hydrochloride |
| 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 Hydrochloride
| Product NDC: | 0378-7065 |
| Labeler Name: | Mylan Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040569 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091102 |
Package Information of Propoxyphene Hydrochloride
| Package NDC: | 0378-7065-01 |
| Package Description: | 100 CAPSULE in 1 BOTTLE, PLASTIC (0378-7065-01) |
NDC Information of Propoxyphene Hydrochloride
| NDC Code | 0378-7065-01 |
| Proprietary Name | Propoxyphene Hydrochloride |
| Package Description | 100 CAPSULE in 1 BOTTLE, PLASTIC (0378-7065-01) |
| Product NDC | 0378-7065 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Propoxyphene Hydrochloride |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20091102 |
| Marketing Category Name | ANDA |
| Labeler Name | Mylan Pharmaceuticals Inc. |
| Substance Name | PROPOXYPHENE HYDROCHLORIDE |
| Strength Number | 65 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
