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Ciprofloxacin Hydrochloride

NDC 83939-0002, Ciprofloxacin Hydrochloride, tablet, film coated, from VERITYRX, LLC.

Product NDC
83939-0002
Status
Listed
Labeler
VERITYRX, 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/83939-0002 \
  -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
83939-0002-1839390002011 TABLET, FILM COATED in 1 POUCH (83939-0002-1)
83939-0002-28393900020250 POUCH in 1 BOX, UNIT-DOSE (83939-0002-2) / 1 TABLET, FILM COATED in 1 POUCH
83939-0002-383939000203100 POUCH in 1 BOX, UNIT-DOSE (83939-0002-3) / 1 TABLET, FILM COATED in 1 POUCH

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/42542f65-84a7-fdab-e063-6394a90a1095

Use it

Look up 83939-0002 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/83939-0002 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 83939-0002. 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.