Package 50742-115-01
Brand: desipramine hydrochloride
Generic: desipramine hydrochloridePackage Facts
Identity
Package NDC
50742-115-01
Digits Only
5074211501
Product NDC
50742-115
Description
100 TABLET in 1 BOTTLE (50742-115-01)
Marketing
Marketing Status
Brand
desipramine hydrochloride
Generic
desipramine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7a0e5dd9-7456-4774-b529-ce9d5627b654", "openfda": {"upc": ["0350742112012", "0350742116010", "0350742114016", "0350742117505", "0350742113019", "0350742115013"], "unii": ["1Y58DO4MY1"], "rxcui": ["1099288", "1099292", "1099296", "1099300", "1099304", "1099316"], "spl_set_id": ["7280f157-3fff-41c5-b3f4-510b8bacdaba"], "manufacturer_name": ["Ingenus Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (50742-115-01)", "package_ndc": "50742-115-01", "marketing_start_date": "20180919"}], "brand_name": "DESIPRAMINE HYDROCHLORIDE", "product_id": "50742-115_7a0e5dd9-7456-4774-b529-ce9d5627b654", "dosage_form": "TABLET", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "50742-115", "generic_name": "desipramine hydrochloride", "labeler_name": "Ingenus Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DESIPRAMINE HYDROCHLORIDE", "active_ingredients": [{"name": "DESIPRAMINE HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA204963", "marketing_category": "ANDA", "marketing_start_date": "20180919", "listing_expiration_date": "20261231"}