angeliq
Generic: drospirenone and estradiol
Labeler: bayer healthcare pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
angeliq
Generic Name
drospirenone and estradiol
Labeler
bayer healthcare pharmaceuticals inc.
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
drospirenone .25 mg/1, estradiol .5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50419-482
Product ID
50419-482_261d4ace-5c4e-48f6-b793-354492017e89
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA021355
Listing Expiration
2027-12-31
Marketing Start
2012-02-29
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
50419482
Hyphenated Format
50419-482
Supplemental Identifiers
RxCUI
UNII
NUI
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
angeliq (source: ndc)
Generic Name
drospirenone and estradiol (source: ndc)
Application Number
NDA021355 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .25 mg/1
- .5 mg/1
Packaging
- 3 BLISTER PACK in 1 CARTON (50419-482-03) / 28 TABLET, FILM COATED in 1 BLISTER PACK (50419-482-01)
- 1 BLISTER PACK in 1 CARTON (50419-482-72) / 14 TABLET, FILM COATED in 1 BLISTER PACK (50419-482-71)
Packages (2)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "261d4ace-5c4e-48f6-b793-354492017e89", "openfda": {"nui": ["M0447349", "N0000175602", "M0447348", "N0000175825", "N0000000100"], "unii": ["N295J34A25", "4TI98Z838E"], "rxcui": ["1483549", "1483550", "1483551", "1483552", "1483553", "1483554"], "spl_set_id": ["761834c2-6b61-4583-84c2-f1ca4a97c4f2"], "pharm_class_cs": ["Progesterone Congeners [CS]", "Estradiol Congeners [CS]"], "pharm_class_epc": ["Progestin [EPC]", "Estrogen [EPC]"], "pharm_class_moa": ["Estrogen Receptor Agonists [MoA]"], "manufacturer_name": ["Bayer HealthCare Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 CARTON (50419-482-03) / 28 TABLET, FILM COATED in 1 BLISTER PACK (50419-482-01)", "package_ndc": "50419-482-03", "marketing_start_date": "20120229"}, {"sample": false, "description": "1 BLISTER PACK in 1 CARTON (50419-482-72) / 14 TABLET, FILM COATED in 1 BLISTER PACK (50419-482-71)", "package_ndc": "50419-482-72", "marketing_start_date": "20120229"}], "brand_name": "Angeliq", "product_id": "50419-482_261d4ace-5c4e-48f6-b793-354492017e89", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Estradiol Congeners [CS]", "Estrogen Receptor Agonists [MoA]", "Estrogen [EPC]", "Progesterone Congeners [CS]", "Progestin [EPC]"], "product_ndc": "50419-482", "generic_name": "drospirenone and estradiol", "labeler_name": "Bayer HealthCare Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Angeliq", "active_ingredients": [{"name": "DROSPIRENONE", "strength": ".25 mg/1"}, {"name": "ESTRADIOL", "strength": ".5 mg/1"}], "application_number": "NDA021355", "marketing_category": "NDA", "marketing_start_date": "20120229", "listing_expiration_date": "20271231"}