Ciprofloxacin

NDC 68071-3737, Ciprofolxacin, tablet, from NuCare Pharmaceutical, Inc..

Product NDC: 68071-3737
Status: Listed
Labeler: NuCare Pharmaceutical, 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/68071-3737 \
  -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 NDC	NDC-11	Package
68071-3737-2	68071373702	2 TABLET in 1 BOTTLE (68071-3737-2)
68071-3737-4	68071373704	4 TABLET in 1 BOTTLE (68071-3737-4)
68071-3737-6	68071373706	6 TABLET in 1 BOTTLE (68071-3737-6)

Linked data

RxNorm, label and prices

RxNorm concepts

309309ciprofloxacin 500 MG Oral Tablet (SCD)

Related lookups

FDA label sections
GET /v1/drugs/labels/288ea7b2-ecf2-e8e0-e063-6294a90a306a

Use it

Look up 68071-3737 from code or an agent

curl

curl https://api.healthcare.dev/v1/drugs/ndc/68071-3737 \
  -H "Authorization: Bearer $HDEV_API_KEY"

MCP prompt

Using the healthcare.dev MCP server, look up NDC 68071-3737. 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.