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Cuprimine
Cuprimine - 25010-705-15 - (Penicillamine)
Drug Information of Cuprimine
| Product NDC: | 25010-705 |
| Proprietary Name: | Cuprimine |
| Non Proprietary Name: | Penicillamine |
| Active Ingredient(s): | 250 mg/1 & nbsp; Penicillamine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cuprimine
| Product NDC: | 25010-705 |
| Labeler Name: | Aton Pharma, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019853 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19701204 |
Package Information of Cuprimine
| Package NDC: | 25010-705-15 |
| Package Description: | 100 CAPSULE in 1 BOTTLE (25010-705-15) |
NDC Information of Cuprimine
| NDC Code | 25010-705-15 |
| Proprietary Name | Cuprimine |
| Package Description | 100 CAPSULE in 1 BOTTLE (25010-705-15) |
| Product NDC | 25010-705 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Penicillamine |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 19701204 |
| Marketing Category Name | NDA |
| Labeler Name | Aton Pharma, Inc. |
| Substance Name | PENICILLAMINE |
| Strength Number | 250 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Antirheumatic Agent [EPC] |
