Package 68462-852-29

Brand: charlotte 24fe

Generic: norethindrone acetate and ethinyl estradiol and ferrous fumarate
NDC Package

Package Facts

Identity

Package NDC 68462-852-29
Digits Only 6846285229
Product NDC 68462-852
Description

3 BLISTER PACK in 1 CARTON (68462-852-29) / 1 KIT in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2020-02-20
Brand charlotte 24fe
Generic norethindrone acetate and ethinyl estradiol and ferrous fumarate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"spl_id": "d5dfc9ba-16e2-4a8f-babf-b4a159785d47", "openfda": {"upc": ["0368462852293"], "rxcui": ["259176", "1426288", "1426600", "2280761"], "spl_set_id": ["b01f8921-8844-43e6-8167-561ff03c21ef"], "manufacturer_name": ["Glenmark Pharmaceuticals Inc., USA"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 CARTON (68462-852-29)  / 1 KIT in 1 BLISTER PACK", "package_ndc": "68462-852-29", "marketing_start_date": "20200220"}], "brand_name": "Charlotte 24Fe", "product_id": "68462-852_d5dfc9ba-16e2-4a8f-babf-b4a159785d47", "dosage_form": "KIT", "product_ndc": "68462-852", "generic_name": "norethindrone acetate and ethinyl estradiol and ferrous fumarate", "labeler_name": "Glenmark Pharmaceuticals Inc., USA", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Charlotte 24Fe", "application_number": "ANDA210369", "marketing_category": "ANDA", "marketing_start_date": "20200220", "listing_expiration_date": "20271231"}