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Ciprofloxacin Hydrochloride

NDC 69367-387, Ciprofloxacin Hydrochloride, tablet, film coated, from Westminster Pharmaceuticals, LLC.

Product NDC
69367-387
Status
Listed
Labeler
Westminster Pharmaceuticals, LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA076593
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69367-387 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CIPROFLOXACIN HYDROCHLORIDE750 mg/1

Pharmacologic classes

Cytochrome P450 1A2 Inhibitors [MoA]; Fluoroquinolone Antibacterial [EPC]; Fluoroquinolones [CS]

Package NDCNDC-11Package
69367-387-506936703875050 TABLET, FILM COATED in 1 BOTTLE (69367-387-50)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c47250c2-bece-46b5-8b3b-b7c97d9005d8
  • NADAC price for package 69367038750

    GET /v1/drugs/nadac/69367038750

Use it

Look up 69367-387 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69367-387 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69367-387. 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.