Package 75907-086-28

Brand: tilia fe

Generic: ndac and ee tablets and ferrous fumarate tablets
NDC Package

Package Facts

Identity

Package NDC 75907-086-28
Digits Only 7590708628
Product NDC 75907-086
Product ID 75907-086_af37ed43-957f-4f93-935c-6c2158ab0e15
Description

1 BLISTER PACK in 1 PACKET (75907-086-28) / 1 KIT in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2024-06-01
Brand tilia fe
Generic ndac and ee tablets and ferrous fumarate tablets
Sample Package No

Linked Drug Pages (1)

Tilia Fe ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "af37ed43-957f-4f93-935c-6c2158ab0e15", "openfda": {"rxcui": ["259176", "1358762", "1359130", "1359131", "1359132", "1359134"], "spl_set_id": ["118fb017-b44d-4223-ac5a-501ca96de210"], "manufacturer_name": ["Dr. Reddys Laboratories Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 PACKET (75907-086-28)  / 1 KIT in 1 BLISTER PACK", "package_ndc": "75907-086-28", "marketing_start_date": "20240601"}, {"sample": false, "description": "3 BLISTER PACK in 1 CARTON (75907-086-32)  / 1 KIT in 1 BLISTER PACK", "package_ndc": "75907-086-32", "marketing_start_date": "20240601"}], "brand_name": "Tilia Fe", "product_id": "75907-086_af37ed43-957f-4f93-935c-6c2158ab0e15", "dosage_form": "KIT", "product_ndc": "75907-086", "generic_name": "NdAc and EE Tablets and Ferrous Fumarate Tablets", "labeler_name": "Dr. Reddys Laboratories Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tilia Fe", "application_number": "ANDA202962", "marketing_category": "ANDA", "marketing_start_date": "20240601", "listing_expiration_date": "20261231"}