norethindrone acetate and ethinyl estradiol
Generic: norethindrone acetate and ethinyl estradiol
Labeler: mylan pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
norethindrone acetate and ethinyl estradiol
Generic Name
norethindrone acetate and ethinyl estradiol
Labeler
mylan pharmaceuticals inc.
Dosage Form
KIT
Manufacturer
Identifiers & Regulatory
Product NDC
0378-7283
Product ID
0378-7283_024ab85d-682d-b3cb-9886-57dd821426c8
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA202772
Listing Expiration
2026-12-31
Marketing Start
2014-07-16
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
03787283
Hyphenated Format
0378-7283
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 (source: ndc)
Generic Name
norethindrone acetate and ethinyl estradiol (source: ndc)
Application Number
ANDA202772 (source: ndc)
Resolved Composition
Strengths
- 1 mg/0.02 mg
- 75 mg
Packaging
- 3 POUCH in 1 CARTON (0378-7283-53) / 1 BLISTER PACK in 1 POUCH (0378-7283-85) / 1 KIT in 1 BLISTER PACK
Packages (1)
Ingredients (0)
No ingredient records.
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"spl_id": "024ab85d-682d-b3cb-9886-57dd821426c8", "openfda": {"rxcui": ["259176", "1358762", "1358763"], "spl_set_id": ["2376cab5-3d34-4a0a-9ba1-df19a96eb5dd"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 POUCH in 1 CARTON (0378-7283-53) / 1 BLISTER PACK in 1 POUCH (0378-7283-85) / 1 KIT in 1 BLISTER PACK", "package_ndc": "0378-7283-53", "marketing_start_date": "20140716"}], "brand_name": "NORETHINDRONE ACETATE AND ETHINYL ESTRADIOL", "product_id": "0378-7283_024ab85d-682d-b3cb-9886-57dd821426c8", "dosage_form": "KIT", "product_ndc": "0378-7283", "generic_name": "norethindrone acetate and ethinyl estradiol", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NORETHINDRONE ACETATE AND ETHINYL ESTRADIOL", "application_number": "ANDA202772", "marketing_category": "ANDA", "marketing_start_date": "20140716", "listing_expiration_date": "20261231"}