Benzonatate NDC 71335-1968

Product information

Brand name (proprietary)

Benzonatate

Generic name (nonproprietary)

benzonatate

Active ingredients

Benzonatate — 100 mg/1

Dosage form

Capsule

Route

Oral

Labeler

Bryant Ranch Prepack

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 202765

Marketing start

Sep 7, 2017

Listing expires

Dec 31, 2026

Other FDA classes

Decreased Tracheobronchial Stretch Receptor Activity (Physiologic effect)

Identifiers

Product ID 71335-1968_db58683b-93e6-49ac-a724-7ca687e17feeSPL ID db58683b-93e6-49ac-a724-7ca687e17feeSPL set ID 5add9fd2-5f54-4669-b82a-0e0a8fcd5a8fRxCUI 197397UNII 5P4DHS6ENR

Pharmacologic class

Non-narcotic Antitussive

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

N471335196800 followed by a unit qualifier and the quantity Copy

Package 71335-1968-00. 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 202765

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

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