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Sotalol Hydrochloride

NDC 69584-842, Sotalol Hydrochloride, tablet, from Oxford Pharmaceuticals, LLC.

Product NDC
69584-842
Status
Listed
Labeler
Oxford Pharmaceuticals, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA075563
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69584-842 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SOTALOL HYDROCHLORIDE120 mg/1

Pharmacologic classes

Adrenergic beta-Antagonists [MoA]; Antiarrhythmic [EPC]; Cardiac Rhythm Alteration [PE]

Package NDCNDC-11Package
69584-842-1069584084210100 TABLET in 1 BOTTLE (69584-842-10)
69584-842-3069584084230300 TABLET in 1 BOTTLE (69584-842-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c8ac6351-b1e9-4dd2-82f2-5980814fda15

  • NADAC price for package 69584084210

    GET /v1/drugs/nadac/69584084210

  • NADAC price for package 69584084230

    GET /v1/drugs/nadac/69584084230

Use it

Look up 69584-842 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69584-842 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69584-842. 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.