norethindrone acetate and ethinyl estradiol and ferrous fumarate
Generic: norethindrone acetate and ethinyl estradiol and ferrous fumarate
Labeler: amneal pharmaceuticals ny llcDrug Facts
Product Profile
Brand Name
norethindrone acetate and ethinyl estradiol and ferrous fumarate
Generic Name
norethindrone acetate and ethinyl estradiol and ferrous fumarate
Labeler
amneal pharmaceuticals ny llc
Dosage Form
KIT
Manufacturer
Identifiers & Regulatory
Product NDC
60219-1031
Product ID
60219-1031_ae13db8f-27e2-420a-b909-99d0347e6286
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA207514
Listing Expiration
2026-12-31
Marketing Start
2017-09-21
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
602191031
Hyphenated Format
60219-1031
Supplemental Identifiers
RxCUI
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
norethindrone acetate and ethinyl estradiol and ferrous fumarate (source: ndc)
Generic Name
norethindrone acetate and ethinyl estradiol and ferrous fumarate (source: ndc)
Application Number
ANDA207514 (source: ndc)
Resolved Composition
Strengths
- 1 mg
- 20 mcg
- 75 mg
- 1 mg/20 mcg
Packaging
- 3 BLISTER PACK in 1 CARTON (60219-1031-7) / 1 KIT in 1 BLISTER PACK (60219-1031-6)
Packages (1)
Ingredients (0)
No ingredient records.
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"spl_id": "ae13db8f-27e2-420a-b909-99d0347e6286", "openfda": {"rxcui": ["259176", "1358762", "1359117", "1426288"], "spl_set_id": ["d4fa03d8-0ae0-497f-ba4e-76f03fd7a3ab"], "manufacturer_name": ["Amneal Pharmaceuticals NY LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 CARTON (60219-1031-7) / 1 KIT in 1 BLISTER PACK (60219-1031-6)", "package_ndc": "60219-1031-7", "marketing_start_date": "20170921"}], "brand_name": "Norethindrone Acetate and Ethinyl Estradiol and Ferrous Fumarate", "product_id": "60219-1031_ae13db8f-27e2-420a-b909-99d0347e6286", "dosage_form": "KIT", "product_ndc": "60219-1031", "generic_name": "Norethindrone Acetate and Ethinyl Estradiol and Ferrous Fumarate", "labeler_name": "Amneal Pharmaceuticals NY LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Norethindrone Acetate and Ethinyl Estradiol and Ferrous Fumarate", "application_number": "ANDA207514", "marketing_category": "ANDA", "marketing_start_date": "20170921", "listing_expiration_date": "20261231"}