Package 69452-149-20

Brand: progesterone

Generic: progesterone
NDC Package

Package Facts

Identity

Package NDC 69452-149-20
Digits Only 6945214920
Product NDC 69452-149
Description

100 CAPSULE in 1 BOTTLE (69452-149-20)

Marketing

Marketing Status
Marketed Since 2016-09-20
Brand progesterone
Generic progesterone
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "73113fdd-1ff9-419e-8c29-3e82c8898cce", "openfda": {"nui": ["M0017672", "N0000175601"], "unii": ["4G7DS2Q64Y"], "rxcui": ["260243", "312641"], "spl_set_id": ["3acad9b0-7ec6-4d5e-9852-32ffadbbed6d"], "pharm_class_cs": ["Progesterone [CS]"], "pharm_class_epc": ["Progesterone [EPC]"], "manufacturer_name": ["Bionpharma Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (69452-149-20)", "package_ndc": "69452-149-20", "marketing_start_date": "20160920"}], "brand_name": "PROGESTERONE", "product_id": "69452-149_73113fdd-1ff9-419e-8c29-3e82c8898cce", "dosage_form": "CAPSULE", "pharm_class": ["Progesterone [CS]", "Progesterone [EPC]"], "product_ndc": "69452-149", "generic_name": "PROGESTERONE", "labeler_name": "Bionpharma Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PROGESTERONE", "active_ingredients": [{"name": "PROGESTERONE", "strength": "200 mg/1"}], "application_number": "ANDA200900", "marketing_category": "ANDA", "marketing_start_date": "20160920", "listing_expiration_date": "20261231"}