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PHYTONADIONE

NDC 70095-154, Phytonadione, injection, emulsion, from Sun Pharmaceutical Industries, Inc..

Product NDC
70095-154
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
INJECTION, EMULSION
Route
INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA216298
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70095-154 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PHYTONADIONE1 mg/.5mL

Pharmacologic classes

Increased Prothrombin Activity [PE]; Reversed Anticoagulation Activity [PE]; Vitamin K [CS]; Vitamin K [EPC]; Warfarin Reversal Agent [EPC]

Package NDCNDC-11Package
70095-154-027009501540210 CARTON in 1 CARTON (70095-154-02) / 1 BLISTER PACK in 1 CARTON (70095-154-01) / 1 SYRINGE in 1 BLISTER PACK / .5 mL in 1 SYRINGE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/51c175dd-02f9-68d1-e063-6294a90a4b36

Use it

Look up 70095-154 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70095-154 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70095-154. 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.