Package 60505-4896-1

Brand: desogestrel and ethinyl estradiol

Generic: desogestrel and ethinyl estradiol
NDC Package

Package Facts

Identity

Package NDC 60505-4896-1
Digits Only 6050548961
Product NDC 60505-4896
Description

3 BLISTER PACK in 1 CARTON (60505-4896-1) / 1 KIT in 1 BLISTER PACK * 21 TABLET in 1 BLISTER PACK * 7 TABLET in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2026-02-05
Brand desogestrel and ethinyl estradiol
Generic desogestrel and ethinyl estradiol
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"spl_id": "49718fe6-b8d0-6db9-e063-6294a90aa923", "openfda": {"rxcui": ["240707", "748797", "749848"], "spl_set_id": ["9bb13b85-5d54-4689-b915-50b1da3a525b"], "manufacturer_name": ["Apotex Corp."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 CARTON (60505-4896-1)  / 1 KIT in 1 BLISTER PACK *  21 TABLET in 1 BLISTER PACK *  7 TABLET in 1 BLISTER PACK", "package_ndc": "60505-4896-1", "marketing_start_date": "20260205"}], "brand_name": "desogestrel and ethinyl estradiol", "product_id": "60505-4896_49718fe6-b8d0-6db9-e063-6294a90aa923", "dosage_form": "KIT", "product_ndc": "60505-4896", "generic_name": "desogestrel and ethinyl estradiol", "labeler_name": "Apotex Corp.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "desogestrel and ethinyl estradiol", "application_number": "ANDA207067", "marketing_category": "ANDA", "marketing_start_date": "20260205", "listing_expiration_date": "20271231"}