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PROPOFOL

NDC 0641-6196, PROPOFOL, injection, emulsion, from Hikma Pharmaceuticals USA Inc..

Product NDC
0641-6196
Status
Listed
Labeler
Hikma Pharmaceuticals USA Inc.
Dosage form
INJECTION, EMULSION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA074848
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0641-6196 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PROPOFOL10 mg/mL

Pharmacologic classes

General Anesthesia [PE]; General Anesthetic [EPC]

Package NDCNDC-11Package
0641-6196-100064161961010 VIAL, SINGLE-USE in 1 CARTON (0641-6196-10) / 100 mL in 1 VIAL, SINGLE-USE (0641-6196-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/fdb77e13-f5a7-4c4a-9f8e-338b702239c8

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=0641-6196

Use it

Look up 0641-6196 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0641-6196 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0641-6196. 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.