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Sotalol Hydrochloride

NDC 51655-450, Sotalol Hydrochloride, tablet, from Northwind Health Company, LLC.

Product NDC
51655-450
Status
Listed
Labeler
Northwind Health Company, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA076140
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51655-450 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SOTALOL HYDROCHLORIDE240 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
51655-450-155165504501550 TABLET in 1 BOTTLE, PLASTIC (51655-450-15)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/fe82c866-03d4-e07b-e053-6394a90a8b1e

Use it

Look up 51655-450 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51655-450 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51655-450. 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.