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Fluoxetine Hydrochloride

NDC 68180-997, Fluoxetine Hydrochloride, tablet, from Lupin Pharmaceuticals, Inc..

Product NDC
68180-997
Status
Listed
Labeler
Lupin Pharmaceuticals, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA211632
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68180-997 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FLUOXETINE HYDROCHLORIDE60 mg/1

Pharmacologic classes

Serotonin Reuptake Inhibitor [EPC]; Serotonin Uptake Inhibitors [MoA]

Package NDCNDC-11Package
68180-997-066818009970630 TABLET in 1 BOTTLE (68180-997-06)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f274f102-67ec-46e7-b248-533be2e3003b

Use it

Look up 68180-997 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68180-997 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68180-997. 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.