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Propranolol Hydrochloride

NDC 70518-3552, propranolol hydrochloride, capsule, extended release, from REMEDYREPACK INC..

Product NDC
70518-3552
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
CAPSULE, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA212026
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3552 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PROPRANOLOL HYDROCHLORIDE80 mg/1

Pharmacologic classes

Adrenergic beta-Antagonists [MoA]; beta-Adrenergic Blocker [EPC]

Package NDCNDC-11Package
70518-3552-07051835520090 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-3552-0)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/414c4b69-38a1-4220-bec8-204c9a624b85

Use it

Look up 70518-3552 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3552 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-3552. 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.