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Olanzapine

NDC 70518-1635, Olanzapine, tablet, film coated, from REMEDYREPACK INC..

Product NDC
70518-1635
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA076255
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-1635 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • OLANZAPINE10 mg/1

Pharmacologic classes

Atypical Antipsychotic [EPC]

Package NDCNDC-11Package
70518-1635-07051816350030 TABLET, FILM COATED in 1 BLISTER PACK (70518-1635-0)
70518-1635-17051816350130 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1635-1)
70518-1635-27051816350260 TABLET, FILM COATED in 1 BLISTER PACK (70518-1635-2)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2a7300d3-95e3-427e-bf37-55fa654cc90a

Use it

Look up 70518-1635 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-1635 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-1635. 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.