Package 43386-360-21

Brand: phenelzine sulfate

Generic: phenelzine sulfate
NDC Package

Package Facts

Identity

Package NDC 43386-360-21
Digits Only 4338636021
Product NDC 43386-360
Description

60 TABLET in 1 BOTTLE (43386-360-21)

Marketing

Marketing Status
Marketed Since 2011-02-14
Brand phenelzine sulfate
Generic phenelzine sulfate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1eb0b695-ce65-45c2-914a-87bc2105b139", "openfda": {"upc": ["0343386360215"], "unii": ["2681D7P965"], "rxcui": ["312347"], "spl_set_id": ["40483372-448f-4284-976c-8462ef256661"], "manufacturer_name": ["Lupin Pharmaceuticals,Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (43386-360-21)", "package_ndc": "43386-360-21", "marketing_start_date": "20110214"}], "brand_name": "Phenelzine Sulfate", "product_id": "43386-360_1eb0b695-ce65-45c2-914a-87bc2105b139", "dosage_form": "TABLET", "pharm_class": ["Monoamine Oxidase Inhibitor [EPC]", "Monoamine Oxidase Inhibitors [MoA]"], "product_ndc": "43386-360", "generic_name": "Phenelzine Sulfate", "labeler_name": "Lupin Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phenelzine Sulfate", "active_ingredients": [{"name": "PHENELZINE SULFATE", "strength": "15 mg/1"}], "application_number": "ANDA200181", "marketing_category": "ANDA", "marketing_start_date": "20101214", "listing_expiration_date": "20261231"}