Package 68788-8719-3

Brand: progesterone

Generic: progesterone
NDC Package

Package Facts

Identity

Package NDC 68788-8719-3
Digits Only 6878887193
Product NDC 68788-8719
Description

30 CAPSULE in 1 BOTTLE (68788-8719-3)

Marketing

Marketing Status
Marketed Since 2024-07-26
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": "669c35d3-43cd-48b6-b450-42fe5717f04b", "openfda": {"nui": ["M0017672", "N0000175601"], "unii": ["4G7DS2Q64Y"], "rxcui": ["312641"], "spl_set_id": ["41c9546c-a854-4395-9506-d1be61f4e60f"], "pharm_class_cs": ["Progesterone [CS]"], "pharm_class_epc": ["Progesterone [EPC]"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (68788-8719-3)", "package_ndc": "68788-8719-3", "marketing_start_date": "20240726"}], "brand_name": "PROGESTERONE", "product_id": "68788-8719_669c35d3-43cd-48b6-b450-42fe5717f04b", "dosage_form": "CAPSULE", "pharm_class": ["Progesterone [CS]", "Progesterone [EPC]"], "product_ndc": "68788-8719", "generic_name": "PROGESTERONE", "labeler_name": "Preferred Pharmaceuticals 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": "20240726", "listing_expiration_date": "20261231"}