estrogens, conjugated

Generic: estrogens, conjugated

Labeler: ingenus pharmaceuticals, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name estrogens, conjugated
Generic Name estrogens, conjugated
Labeler ingenus pharmaceuticals, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

estrogens, conjugated .9 mg/1

Manufacturer
Ingenus Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 50742-390
Product ID 50742-390_11c5dbc7-30bb-482c-bac7-4c94b72c44ee
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214023
Listing Expiration 2026-12-31
Marketing Start 2025-10-16

Pharmacologic Class

Established (EPC)
estrogen [epc]
Mechanism of Action
estrogen receptor agonists [moa]
Chemical Structure
estrogens, conjugated (usp) [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 50742390
Hyphenated Format 50742-390

Supplemental Identifiers

RxCUI
197661 197662
UNII
IU5QR144QX
NUI
N0000175825 N0000000100 M0007792

Packaging Origin

Original Packager
true

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 estrogens, conjugated (source: ndc)
Generic Name estrogens, conjugated (source: ndc)
Application Number ANDA214023 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .9 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (50742-390-01)
  • 1000 TABLET, FILM COATED in 1 BOTTLE (50742-390-10)
source: ndc

Packages (2)

Ingredients (1)

estrogens, conjugated (.9 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "11c5dbc7-30bb-482c-bac7-4c94b72c44ee", "openfda": {"nui": ["N0000175825", "N0000000100", "M0007792"], "unii": ["IU5QR144QX"], "rxcui": ["197661", "197662"], "spl_set_id": ["7277bab4-d8c2-4e4b-a0d9-5dfe1885d547"], "pharm_class_cs": ["Estrogens, Conjugated (USP) [CS]"], "pharm_class_epc": ["Estrogen [EPC]"], "pharm_class_moa": ["Estrogen Receptor Agonists [MoA]"], "manufacturer_name": ["Ingenus Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (50742-390-01)", "package_ndc": "50742-390-01", "marketing_start_date": "20251016"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (50742-390-10)", "package_ndc": "50742-390-10", "marketing_start_date": "20251016"}], "brand_name": "estrogens, conjugated", "product_id": "50742-390_11c5dbc7-30bb-482c-bac7-4c94b72c44ee", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Estrogen Receptor Agonists [MoA]", "Estrogen [EPC]", "Estrogens", "Conjugated (USP) [CS]"], "product_ndc": "50742-390", "generic_name": "estrogens, conjugated", "labeler_name": "Ingenus Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "estrogens, conjugated", "active_ingredients": [{"name": "ESTROGENS, CONJUGATED", "strength": ".9 mg/1"}], "application_number": "ANDA214023", "marketing_category": "ANDA", "marketing_start_date": "20251016", "listing_expiration_date": "20261231"}