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Premarin

NDC 0046-1101, estrogens, conjugated, tablet, film coated, from Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc..

Product NDC
0046-1101
Status
Listed
Labeler
Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA004782
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0046-1101 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ESTROGENS, CONJUGATED.45 mg/1

Pharmacologic classes

Estrogen Receptor Agonists [MoA]; Estrogen [EPC]; Estrogens, Conjugated (USP) [CS]

Package NDCNDC-11Package
0046-1101-8100046110181100 TABLET, FILM COATED in 1 BOTTLE (0046-1101-81)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/258e1602-a3cf-4ccc-ca80-73dbbfb812ff

  • NADAC price for package 00046110181

    GET /v1/drugs/nadac/00046110181

Use it

Look up 0046-1101 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0046-1101 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0046-1101. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.