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Ciprofloxacin

NDC 68071-3901, Ciprofolxacin, tablet, from NuCare Pharmaceuticals,Inc..

Product NDC
68071-3901
Status
Listed
Labeler
NuCare Pharmaceuticals,Inc.
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/68071-3901 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CIPROFLOXACIN HYDROCHLORIDE250 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
68071-3901-168071390101100 TABLET in 1 BOTTLE (68071-3901-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/41206a0f-7a5b-6a12-e063-6394a90a58b1

Use it

Look up 68071-3901 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68071-3901 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68071-3901. 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.