Package 58657-151-10

Brand: folic acid

Generic: folic acid
NDC Package

Package Facts

Identity

Package NDC 58657-151-10
Digits Only 5865715110
Product NDC 58657-151
Product ID 58657-151_41b4d71d-2dc2-36bd-e063-6294a90af1e1
Description

1000 TABLET in 1 BOTTLE (58657-151-10)

Marketing

Marketing Status
Marketed Since 2021-01-25
Brand folic acid
Generic folic acid
Sample Package No

Linked Drug Pages (1)

Folic Acid ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "41b4d71d-2dc2-36bd-e063-6294a90af1e1", "openfda": {"unii": ["935E97BOY8"], "rxcui": ["310410"], "spl_set_id": ["b9c315ff-cecb-8b75-e053-2995a90aa204"], "manufacturer_name": ["Method Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (58657-151-01)", "package_ndc": "58657-151-01", "marketing_start_date": "20210125"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (58657-151-10)", "package_ndc": "58657-151-10", "marketing_start_date": "20210125"}], "brand_name": "Folic Acid", "product_id": "58657-151_41b4d71d-2dc2-36bd-e063-6294a90af1e1", "dosage_form": "TABLET", "product_ndc": "58657-151", "generic_name": "Folic Acid", "labeler_name": "Method Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Folic Acid", "active_ingredients": [{"name": "FOLIC ACID", "strength": "1 mg/1"}], "application_number": "ANDA211064", "marketing_category": "ANDA", "marketing_start_date": "20180209", "listing_expiration_date": "20261231"}