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Sotalol Hydrochloride

NDC 72789-135, Sotalol Hydrochloride, tablet, from PD-Rx Pharmaceuticals, Inc..

Product NDC
72789-135
Status
Listed
Labeler
PD-Rx Pharmaceuticals, Inc.
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/72789-135 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SOTALOL HYDROCHLORIDE160 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
72789-135-0172789013501100 TABLET in 1 BOTTLE, PLASTIC (72789-135-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e6ea445d-4d7c-4c32-83a7-e7683a56075b

Use it

Look up 72789-135 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72789-135 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72789-135. 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.