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Ciprofloxacin

NDC 16252-515, Ciprofloxacin, tablet, film coated, from Teva Pharmaceuticals USA, Inc..

Product NDC
16252-515
Status
Listed
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA076794
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/16252-515 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CIPROFLOXACIN HYDROCHLORIDE500 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
16252-515-0116252051501100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16252-515-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/3e4402d4-e0d3-9846-3e81-ed46f34137fe

  • NADAC price for package 16252051501

    GET /v1/drugs/nadac/16252051501

Use it

Look up 16252-515 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/16252-515 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 16252-515. 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.