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Mirtazapine

NDC 70954-830, Mirtazapine, tablet, film coated, from ANI Pharmaceuticals, Inc..

Product NDC
70954-830
Status
Listed
Labeler
ANI Pharmaceuticals, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA219919
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70954-830 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MIRTAZAPINE7.5 mg/1
Package NDCNDC-11Package
70954-830-107095408301030 TABLET, FILM COATED in 1 BOTTLE (70954-830-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/bb134141-6069-4b86-abac-7783bf5df60d

  • NADAC price for package 70954083010

    GET /v1/drugs/nadac/70954083010

Use it

Look up 70954-830 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70954-830 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70954-830. 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.