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Mirtazapine

NDC 68788-7251, Mirtazapine, tablet, film coated, from Preferred Pharmaceuticals Inc..

Product NDC
68788-7251
Status
Listed
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA076921
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68788-7251 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MIRTAZAPINE15 mg/1
Package NDCNDC-11Package
68788-7251-16878872510115 TABLET, FILM COATED in 1 BOTTLE (68788-7251-1)
68788-7251-36878872510330 TABLET, FILM COATED in 1 BOTTLE (68788-7251-3)
68788-7251-66878872510660 TABLET, FILM COATED in 1 BOTTLE (68788-7251-6)
68788-7251-96878872510990 TABLET, FILM COATED in 1 BOTTLE (68788-7251-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c22c4325-4f1a-4d12-8039-d3b1263fa3ad

Use it

Look up 68788-7251 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68788-7251 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68788-7251. 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.