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United States · US · US:0046-0749_97a59d56-720c-42fd-86b7-00ad93752452
Premarin
Orange BookUNIISPLATC G03CA57
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerWyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
CountryUS (United States)
ATC codeG03CA57
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1100460749051 VIAL in 1 CARTON (0046-0749-05) / 5 mL in 1 VIAL
Annotations
UNII (FDA Substance ID)
IU5QR144QX
ESTROGENS, CONJUGATED
RxCUI 4099
Orange Book
N010402
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "IU5QR144QX",
"rxcui": "4099",
"inchikey": null,
"display_name": "ESTROGENS, CONJUGATED",
"substance_type": "mixture",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "INTRAMUSCULAR; INTRAVENOUS",
"spl_meta": {
"258e1602-a3cf-4ccc-ca80-73dbbfb812ff": {
"match": "brand_token",
"title": "PREMARIN (ESTROGENS, CONJUGATED) TABLET, FILM COATED [WYETH PHARMACEUTICALS LLC, A SUBSIDIARY OF PFIZER INC.]",
"spl_version": "36",
"published_date": "2026-02-23"
}
},
"productid": "0046-0749_97a59d56-720c-42fd-86b7-00ad93752452",
"productndc": "0046-0749",
"dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION",
"orange_book": {
"appl_no": "010402",
"products": [
{
"rs": true,
"rld": true,
"te_code": null,
"strength": "25MG/VIAL",
"product_no": "001",
"approval_date": "Approved Prior to Jan 1, 1982"
}
],
"appl_type": "N"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "ESTROGENS, CONJUGATED",
"proprietary_name": "Premarin",
"active_ingred_unit": "mg/5mL",
"application_number": "NDA010402",
"marketing_category": "NDA",
"nonproprietary_name": "CONJUGATED ESTROGENS",
"start_marketing_date": "19561201",
"active_numerator_strength": "25"
}Related drugs
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