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Morphine Sulfate

NDC 43386-542, Morphine Sulfate, tablet, film coated, extended release, from Lupin Pharmaceuticals,Inc..

Product NDC
43386-542
Status
Listed
Labeler
Lupin Pharmaceuticals,Inc.
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203602
DEA schedule
CII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/43386-542 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MORPHINE SULFATE60 mg/1

Pharmacologic classes

Full Opioid Agonists [MoA]; Opioid Agonist [EPC]

Package NDCNDC-11Package
43386-542-0143386054201100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (43386-542-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d360a33f-6323-4b10-9e81-07e2813c2dbd

Use it

Look up 43386-542 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/43386-542 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 43386-542. 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.