Package 68462-852-29
Brand: charlotte 24fe
Generic: norethindrone acetate and ethinyl estradiol and ferrous fumaratePackage 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
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"}