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leuprolide acetate

NDC 0121-2106, leuprolide acetate, kit, from PAI Holdings, LLC dba PAI Pharma.

Product NDC
0121-2106
Status
Listed
Labeler
PAI Holdings, LLC dba PAI Pharma
Dosage form
KIT
Route
SUBCUTANEOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA217957
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0121-2106 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

None listed.

Package NDCNDC-11Package
0121-2106-02001212106021 KIT in 1 CARTON (0121-2106-02) * 1 VIAL, MULTI-DOSE in 1 CARTON (0121-1053-02) / 2.8 mL in 1 VIAL, MULTI-DOSE * 1 mL in 1 PACKET (0121-2105-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/19be0b7f-e68a-4547-9e49-b51b12821907

  • NADAC price for package 00121210602

    GET /v1/drugs/nadac/00121210602

Use it

Look up 0121-2106 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0121-2106 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0121-2106. 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.