hailey fe 1/20
Generic: norethindrone acetate and ethinyl estradiol and ferrous fumarate
Labeler: glenmark pharmaceuticals inc., usaDrug Facts
Product Profile
Brand Name
hailey fe 1/20
Generic Name
norethindrone acetate and ethinyl estradiol and ferrous fumarate
Labeler
glenmark pharmaceuticals inc., usa
Dosage Form
KIT
Manufacturer
Identifiers & Regulatory
Product NDC
68462-419
Product ID
68462-419_feb1bb19-095f-41f5-8e21-f291bec04d25
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA206597
Listing Expiration
2027-12-31
Marketing Start
2017-11-21
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68462419
Hyphenated Format
68462-419
Supplemental Identifiers
RxCUI
UPC
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
hailey fe 1/20 (source: ndc)
Generic Name
norethindrone acetate and ethinyl estradiol and ferrous fumarate (source: ndc)
Application Number
ANDA206597 (source: ndc)
Resolved Composition
Strengths
- 1 mg
- 20 mcg
- 75 mg
Packaging
- 3 BLISTER PACK in 1 CARTON (68462-419-29) / 1 KIT in 1 BLISTER PACK (68462-419-84)
Packages (1)
Ingredients (0)
No ingredient records.
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"spl_id": "feb1bb19-095f-41f5-8e21-f291bec04d25", "openfda": {"upc": ["0368462419298"], "rxcui": ["259176", "1358762", "1358763", "1989873"], "spl_set_id": ["72bd59e6-26cb-4c01-9511-586372b768b2"], "manufacturer_name": ["Glenmark Pharmaceuticals Inc., USA"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 CARTON (68462-419-29) / 1 KIT in 1 BLISTER PACK (68462-419-84)", "package_ndc": "68462-419-29", "marketing_start_date": "20171121"}], "brand_name": "HAILEY Fe 1/20", "product_id": "68462-419_feb1bb19-095f-41f5-8e21-f291bec04d25", "dosage_form": "KIT", "product_ndc": "68462-419", "generic_name": "norethindrone acetate and ethinyl estradiol and ferrous fumarate", "labeler_name": "Glenmark Pharmaceuticals Inc., USA", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HAILEY Fe 1/20", "application_number": "ANDA206597", "marketing_category": "ANDA", "marketing_start_date": "20171121", "listing_expiration_date": "20271231"}