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Moxifloxacin Hydrochloride

NDC 70069-081, Moxifloxacin Hydrochloride, solution/ drops, from Somerset Therapeutics, LLC.

Product NDC
70069-081
Status
Listed
Labeler
Somerset Therapeutics, LLC
Dosage form
SOLUTION/ DROPS
Route
OPHTHALMIC
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA209698
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70069-081 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MOXIFLOXACIN HYDROCHLORIDE5 mg/mL

Pharmacologic classes

Fluoroquinolone Antibacterial [EPC]; Fluoroquinolones [CS]

Package NDCNDC-11Package
70069-081-01700690081011 BOTTLE in 1 CARTON (70069-081-01) / 3 mL in 1 BOTTLE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f7c68d49-8c61-4bde-a880-4d78568e5aa0

  • NADAC price for package 70069008101

    GET /v1/drugs/nadac/70069008101

Use it

Look up 70069-081 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70069-081 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70069-081. 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.