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Lansoprazole

NDC 76420-621, Lansoprazole, capsule, delayed release, from Asclemed USA, Inc..

Product NDC
76420-621
Status
Listed
Labeler
Asclemed USA, Inc.
Dosage form
CAPSULE, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA207394
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/76420-621 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LANSOPRAZOLE30 mg/1

Pharmacologic classes

Inhibition Gastric Acid Secretion [PE]; Proton Pump Inhibitor [EPC]; Proton Pump Inhibitors [MoA]

Package NDCNDC-11Package
76420-621-307642006213030 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-621-30)
76420-621-607642006216060 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-621-60)
76420-621-907642006219090 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-621-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/71be1129-8562-476e-9d9b-99a21cbf52ec

Use it

Look up 76420-621 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/76420-621 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 76420-621. 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.