Package 30698-021-50

Brand: norpramin

Generic: desipramine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 30698-021-50
Digits Only 3069802150
Product NDC 30698-021
Description

50 TABLET, SUGAR COATED in 1 BOTTLE (30698-021-50)

Marketing

Marketing Status
Marketed Since 1964-11-20
Brand norpramin
Generic desipramine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3904bc92-b199-2543-e063-6294a90a81d8", "openfda": {"unii": ["1Y58DO4MY1"], "rxcui": ["1099288", "1099290", "1099292", "1099294", "1099296", "1099298", "1099300", "1099302", "1099304", "1099306", "1099316", "1099318"], "spl_set_id": ["70b562ea-9f21-4e4a-b3ed-0590b2892f6a"], "manufacturer_name": ["Validus Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 TABLET, SUGAR COATED in 1 BOTTLE (30698-021-50)", "package_ndc": "30698-021-50", "marketing_start_date": "19641120"}], "brand_name": "Norpramin", "product_id": "30698-021_3904bc92-b199-2543-e063-6294a90a81d8", "dosage_form": "TABLET, SUGAR COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "30698-021", "generic_name": "desipramine hydrochloride", "labeler_name": "Validus Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Norpramin", "active_ingredients": [{"name": "DESIPRAMINE HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "NDA014399", "marketing_category": "NDA", "marketing_start_date": "19641120", "listing_expiration_date": "20261231"}