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AMANTADINE HYDROCHLORIDE

NDC 71765-009, Amantadine hydrochloride, tablet, from Zhejiang Jutai Pharmaceutical Co., Ltd..

Product NDC
71765-009
Status
Listed
Labeler
Zhejiang Jutai Pharmaceutical Co., Ltd.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA218598
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71765-009 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • AMANTADINE HYDROCHLORIDE100 mg/1

Pharmacologic classes

Influenza A M2 Protein Inhibitor [EPC]; M2 Protein Inhibitors [MoA]

Package NDCNDC-11Package
71765-009-01717650009012 BLISTER PACK in 1 BOX (71765-009-01) / 12 TABLET in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/9c5e0c61-372b-4d1b-8882-e13f6af8fed0

Use it

Look up 71765-009 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71765-009 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71765-009. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.