Package 43393-023-04

Brand: misoprostol

Generic: misoprostol
NDC Package

Package Facts

Identity

Package NDC 43393-023-04
Digits Only 4339302304
Product NDC 43393-023
Description

4 TABLET in 1 BOTTLE (43393-023-04)

Marketing

Marketing Status
Marketed Since 2023-01-01
Brand misoprostol
Generic misoprostol
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f19b951f-2e45-7072-e053-2a95a90ac730", "openfda": {"nui": ["N0000175785", "M0017811"], "upc": ["0343393023042"], "unii": ["0E43V0BB57"], "rxcui": ["317128"], "spl_set_id": ["2f4d6f06-529c-4b54-908a-0db4c18aff67"], "pharm_class_cs": ["Prostaglandins E, Synthetic [CS]"], "pharm_class_epc": ["Prostaglandin E1 Analog [EPC]"], "manufacturer_name": ["GenBioPro, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "4 TABLET in 1 BOTTLE (43393-023-04)", "package_ndc": "43393-023-04", "marketing_start_date": "20230101"}], "brand_name": "Misoprostol", "product_id": "43393-023_f19b951f-2e45-7072-e053-2a95a90ac730", "dosage_form": "TABLET", "pharm_class": ["Prostaglandin E1 Analog [EPC]", "Prostaglandins E", "Synthetic [CS]"], "product_ndc": "43393-023", "generic_name": "Misoprostol", "labeler_name": "GenBioPro, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Misoprostol", "active_ingredients": [{"name": "MISOPROSTOL", "strength": "200 ug/1"}], "application_number": "ANDA076095", "marketing_category": "ANDA", "marketing_start_date": "20230101", "listing_expiration_date": "20261231"}