Propranolol Hydrochloride NDC 71335-1765

Product information

Brand name (proprietary)

Propranolol Hydrochloride

Generic name (nonproprietary)

propranolol hydrochloride

Active ingredients

Propranolol hydrochloride — 60 mg/1

Dosage form

Capsule, Extended release

Route

Oral

Labeler

Bryant Ranch Prepack

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 212026

Marketing start

Jan 6, 2020

Listing expires

Dec 31, 2026

Other FDA classes

Adrenergic beta-Antagonists (Mechanism)

Identifiers

Product ID 71335-1765_ebc207a3-62f9-4f11-a790-8caf04a30feaSPL ID ebc207a3-62f9-4f11-a790-8caf04a30feaSPL set ID ea98fedc-c440-487e-b144-35a8a389a446RxCUI 856535UNII F8A3652H1V

Pharmacologic class

beta-Adrenergic Blocker

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N471335176501 followed by a unit qualifier and the quantity Copy

Package 71335-1765-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 212026

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.