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Ciprofloxacin

NDC 67296-2135, Ciprofolxacin, tablet, from Redpharm Drug.

Product NDC
67296-2135
Status
Listed
Labeler
Redpharm Drug
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA208921
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/67296-2135 \
  -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
67296-2135-16729621350114 TABLET in 1 BOTTLE (67296-2135-1)
67296-2135-26729621350210 TABLET in 1 BOTTLE (67296-2135-2)
67296-2135-36729621350320 TABLET in 1 BOTTLE (67296-2135-3)
67296-2135-6672962135066 TABLET in 1 BOTTLE (67296-2135-6)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/3253a41f-4f0a-5d83-e063-6294a90a890c

Use it

Look up 67296-2135 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/67296-2135 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 67296-2135. 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.