estradiol

Generic: estradiol

Labeler: preferred pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name estradiol
Generic Name estradiol
Labeler preferred pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

estradiol 1 mg/1

Manufacturer
Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-8860
Product ID 68788-8860_72fbd5a8-9c34-4790-84ed-79f5bd3ae0f0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA217334
Listing Expiration 2026-12-31
Marketing Start 2025-04-11

Pharmacologic Class

Established (EPC)
estrogen [epc]
Mechanism of Action
estrogen receptor agonists [moa]
Chemical Structure
estradiol congeners [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687888860
Hyphenated Format 68788-8860

Supplemental Identifiers

RxCUI
197658
UNII
4TI98Z838E
NUI
M0447348 N0000175825 N0000000100

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 estradiol (source: ndc)
Generic Name estradiol (source: ndc)
Application Number ANDA217334 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (68788-8860-1)
  • 30 TABLET in 1 BOTTLE (68788-8860-3)
  • 60 TABLET in 1 BOTTLE (68788-8860-6)
  • 90 TABLET in 1 BOTTLE (68788-8860-9)
source: ndc

Packages (4)

Ingredients (1)

estradiol (1 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "72fbd5a8-9c34-4790-84ed-79f5bd3ae0f0", "openfda": {"nui": ["M0447348", "N0000175825", "N0000000100"], "unii": ["4TI98Z838E"], "rxcui": ["197658"], "spl_set_id": ["72fbd5a8-9c34-4790-84ed-79f5bd3ae0f0"], "pharm_class_cs": ["Estradiol Congeners [CS]"], "pharm_class_epc": ["Estrogen [EPC]"], "pharm_class_moa": ["Estrogen Receptor Agonists [MoA]"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68788-8860-1)", "package_ndc": "68788-8860-1", "marketing_start_date": "20250411"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-8860-3)", "package_ndc": "68788-8860-3", "marketing_start_date": "20250411"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68788-8860-6)", "package_ndc": "68788-8860-6", "marketing_start_date": "20250411"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-8860-9)", "package_ndc": "68788-8860-9", "marketing_start_date": "20250411"}], "brand_name": "Estradiol", "product_id": "68788-8860_72fbd5a8-9c34-4790-84ed-79f5bd3ae0f0", "dosage_form": "TABLET", "pharm_class": ["Estradiol Congeners [CS]", "Estrogen Receptor Agonists [MoA]", "Estrogen [EPC]"], "product_ndc": "68788-8860", "generic_name": "Estradiol", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Estradiol", "active_ingredients": [{"name": "ESTRADIOL", "strength": "1 mg/1"}], "application_number": "ANDA217334", "marketing_category": "ANDA", "marketing_start_date": "20250411", "listing_expiration_date": "20261231"}