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Megestrol Acetate

NDC 0121-1038, Megestrol Acetate, suspension, from PAI Holdings, LLC dba PAI Pharma.

Product NDC
0121-1038
Status
Listed
Labeler
PAI Holdings, LLC dba PAI Pharma
Dosage form
SUSPENSION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077404
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0121-1038 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MEGESTROL ACETATE400 mg/10mL

Pharmacologic classes

Progesterone Congeners [CS]; Progestin [EPC]

Package NDCNDC-11Package
0121-1038-000012110380010 TRAY in 1 CASE (0121-1038-00) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (0121-1038-10)
0121-1038-40001211038404 TRAY in 1 CASE (0121-1038-40) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (0121-1038-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2d5b58cd-cbb1-4f5c-b13f-63185c0f8e31

Use it

Look up 0121-1038 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0121-1038 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0121-1038. 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.