Package 69367-421-01
Brand: pindolol
Generic: pindololPackage Facts
Identity
Package NDC
69367-421-01
Digits Only
6936742101
Product NDC
69367-421
Description
100 TABLET in 1 BOTTLE (69367-421-01)
Marketing
Marketing Status
Brand
pindolol
Generic
pindolol
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "cd3e9748-5b81-47f6-881c-648b3e2c4d3d", "openfda": {"nui": ["N0000000161", "N0000175556"], "unii": ["BJ4HF6IU1D"], "rxcui": ["198104", "198105"], "spl_set_id": ["efdb0189-37b5-45d6-b92c-1157bb9df789"], "pharm_class_epc": ["beta-Adrenergic Blocker [EPC]"], "pharm_class_moa": ["Adrenergic beta-Antagonists [MoA]"], "manufacturer_name": ["Westminster Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (69367-421-01)", "package_ndc": "69367-421-01", "marketing_start_date": "20251118"}], "brand_name": "Pindolol", "product_id": "69367-421_cd3e9748-5b81-47f6-881c-648b3e2c4d3d", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "69367-421", "generic_name": "Pindolol", "labeler_name": "Westminster Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pindolol", "active_ingredients": [{"name": "PINDOLOL", "strength": "5 mg/1"}], "application_number": "ANDA205415", "marketing_category": "ANDA", "marketing_start_date": "20251118", "listing_expiration_date": "20261231"}