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Fluoxetine

NDC 77771-113, Fluoxetine Hydrochloride, capsule, from RADHA PHARMACEUTICALS, INC..

Product NDC
77771-113
Status
Listed
Labeler
RADHA PHARMACEUTICALS, INC.
Dosage form
CAPSULE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA204597
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/77771-113 \
  -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
77771-113-0177771011301100 CAPSULE in 1 BOTTLE (77771-113-01)
77771-113-10777710113101000 CAPSULE in 1 BOTTLE (77771-113-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1a07ebe9-3661-4a48-b8af-9b228875166a

Use it

Look up 77771-113 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/77771-113 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 77771-113. 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.