Package 72189-391-30
Brand: desipramine hcl
Generic: desipramine hclPackage Facts
Identity
Package NDC
72189-391-30
Digits Only
7218939130
Product NDC
72189-391
Description
30 TABLET in 1 BOTTLE (72189-391-30)
Marketing
Marketing Status
Brand
desipramine hcl
Generic
desipramine hcl
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2c4cdf7a-45d8-784b-e063-6294a90a82b9", "openfda": {"unii": ["1Y58DO4MY1"], "rxcui": ["1099288"], "spl_set_id": ["ed9d2290-9ad9-ecff-e053-2a95a90a5fd6"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72189-391-30)", "package_ndc": "72189-391-30", "marketing_start_date": "20221116"}], "brand_name": "Desipramine HCL", "product_id": "72189-391_2c4cdf7a-45d8-784b-e063-6294a90a82b9", "dosage_form": "TABLET", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "72189-391", "generic_name": "Desipramine HCL", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Desipramine HCL", "active_ingredients": [{"name": "DESIPRAMINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA204963", "marketing_category": "ANDA", "marketing_start_date": "20221116", "listing_expiration_date": "20261231"}