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Neomycin Sulfate

NDC 73473-901, Neomycin Sulfate, tablet, from Solaris Pharma Corporation.

Product NDC
73473-901
Status
Listed
Labeler
Solaris Pharma Corporation
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA065220
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/73473-901 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • NEOMYCIN SULFATE500 mg/1

Pharmacologic classes

Aminoglycoside Antibacterial [EPC]; Aminoglycosides [CS]

Package NDCNDC-11Package
73473-901-0573473090105100 TABLET in 1 BOTTLE, PLASTIC (73473-901-05)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f430c5d9-ae82-3314-e053-2a95a90af04c

  • NADAC price for package 73473090105

    GET /v1/drugs/nadac/73473090105

Use it

Look up 73473-901 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/73473-901 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 73473-901. 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.