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Propranolol Hydrochloride

NDC 82619-135, Propranolol Hydrochloride, capsule, extended release, from Creekwood Pharmaceuticals LLC.

Product NDC
82619-135
Status
Listed
Labeler
Creekwood Pharmaceuticals LLC
Dosage form
CAPSULE, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA219460
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/82619-135 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PROPRANOLOL HYDROCHLORIDE160 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
82619-135-0182619013501100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (82619-135-01)
82619-135-0282619013502500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (82619-135-02)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/289f39f4-ebd3-4fd9-bbb3-72de8124795a

Use it

Look up 82619-135 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/82619-135 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 82619-135. 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.