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NDC 70954-805, Hydroxychloroquine Sulfate, tablet, film coated, from ANI Pharmaceuticals, Inc..

Product NDC
70954-805
Status
Listed
Labeler
ANI Pharmaceuticals, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA214581
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70954-805 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • HYDROXYCHLOROQUINE SULFATE300 mg/1

Pharmacologic classes

Antimalarial [EPC]; Antirheumatic Agent [EPC]

Package NDCNDC-11Package
70954-805-1070954080510100 TABLET, FILM COATED in 1 BOTTLE (70954-805-10)
70954-805-207095408052014 TABLET, FILM COATED in 1 BOTTLE (70954-805-20)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/dd441154-b196-4d4c-bc56-2e37f345ef8d

Use it

Look up 70954-805 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70954-805 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70954-805. 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.