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Fluoxetine Hydrochloride

NDC 68180-998, Fluoxetine Hydrochloride, tablet, from Lupin Pharmaceuticals, Inc..

Product NDC
68180-998
Status
Listed
Labeler
Lupin Pharmaceuticals, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA211653
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68180-998 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FLUOXETINE HYDROCHLORIDE10 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
68180-998-0168180099801100 TABLET in 1 BOTTLE (68180-998-01)
68180-998-066818009980630 TABLET in 1 BOTTLE (68180-998-06)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/dd659085-c32d-4d35-9d4b-bafa2a93f1fb

Use it

Look up 68180-998 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68180-998 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68180-998. 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.