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phenelzine sulfate
phenelzine sulfate - 59762-0119-1 - (Phenelzine Sulfate)
Drug Information of phenelzine sulfate
| Product NDC: | 59762-0119 |
| Proprietary Name: | phenelzine sulfate |
| Non Proprietary Name: | Phenelzine Sulfate |
| Active Ingredient(s): | 15 mg/1 & nbsp; Phenelzine Sulfate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of phenelzine sulfate
| Product NDC: | 59762-0119 |
| Labeler Name: | Greenstone LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA011909 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19610609 |
Package Information of phenelzine sulfate
| Package NDC: | 59762-0119-1 |
| Package Description: | 60 TABLET, FILM COATED in 1 BOTTLE (59762-0119-1) |
NDC Information of phenelzine sulfate
| NDC Code | 59762-0119-1 |
| Proprietary Name | phenelzine sulfate |
| Package Description | 60 TABLET, FILM COATED in 1 BOTTLE (59762-0119-1) |
| Product NDC | 59762-0119 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Phenelzine Sulfate |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 19610609 |
| Marketing Category Name | NDA |
| Labeler Name | Greenstone LLC |
| Substance Name | PHENELZINE SULFATE |
| Strength Number | 15 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Monoamine Oxidase Inhibitor [EPC],Monoamine Oxidase Inhibitors [MoA] |
