Package 60687-572-32
Brand: prazosin hydrochloride
Generic: prazosin hydrochloridePackage Facts
Identity
Package NDC
60687-572-32
Digits Only
6068757232
Product NDC
60687-572
Description
20 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-572-32) / 1 CAPSULE in 1 BLISTER PACK (60687-572-33)
Marketing
Marketing Status
Brand
prazosin hydrochloride
Generic
prazosin hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2b330558-e654-74d6-e063-6394a90a9fd0", "openfda": {"unii": ["X0Z7454B90"], "rxcui": ["198141"], "spl_set_id": ["a2b84746-f780-4e21-adc9-62d09c9363cf"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "20 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-572-32) / 1 CAPSULE in 1 BLISTER PACK (60687-572-33)", "package_ndc": "60687-572-32", "marketing_start_date": "20210421"}], "brand_name": "Prazosin Hydrochloride", "product_id": "60687-572_2b330558-e654-74d6-e063-6394a90a9fd0", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "60687-572", "generic_name": "Prazosin Hydrochloride", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prazosin Hydrochloride", "active_ingredients": [{"name": "PRAZOSIN HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA071745", "marketing_category": "ANDA", "marketing_start_date": "20210421", "listing_expiration_date": "20261231"}