NDC codes

FDA NDC Directory
Product NDC (as listed)71335-3169Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-3169Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
71335-3169-17133531690121 CAPSULE, LIQUID FILLED in 1 BOTTLE (71335-3169-1)Marketed from Aug 11, 2026
71335-3169-271335316902100 CAPSULE, LIQUID FILLED in 1 BOTTLE (71335-3169-2)Marketed from Aug 11, 2026
71335-3169-371335316903500 CAPSULE, LIQUID FILLED in 1 BOTTLE (71335-3169-3)Marketed from Aug 11, 2026
71335-3169-47133531690410 CAPSULE, LIQUID FILLED in 1 BOTTLE (71335-3169-4)Marketed from Aug 11, 2026

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary)
Benzonatate
Generic name (nonproprietary)
benzonatate
Active ingredients
Benzonatate200 mg/1
Dosage form
Capsule, Liquid filled
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 040682
Marketing start
Listing expires
Other FDA classes
Decreased Tracheobronchial Stretch Receptor Activity (Physiologic effect)
Identifiers
Product ID 71335-3169_538a5bfe-55bc-4a5c-8259-f40c4c394d63SPL ID 538a5bfe-55bc-4a5c-8259-f40c4c394d63SPL set ID 0151d970-fd80-482d-ad92-03015eef2618RxCUI 283417UNII 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

N471335316901 followed by a unit qualifier and the quantity

Package 71335-3169-01. 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

Current FDA label (SPL), effective .

Indications (excerpt from the label)

INDICATIONS AND USAGE Benzonatate is indicated for the symptomatic relief of cough.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 040682

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

FDA NDC Directory listings under ANDA 040682
ProductStrengthForm · routeLabelerProduct NDC
BenzonatateBenzonatate 100 mg/1Capsule, Liquid filledOralAmneal Pharmaceuticals LLC65162-536
BenzonatateBenzonatate 200 mg/1Capsule, Liquid filledOralAmneal Pharmaceuticals LLC65162-537
BenzonatateBenzonatate 200 mg/1Capsule, Liquid filledOralRedpharm Drug67296-2202
BenzonatateBenzonatate 100 mg/1Capsule, Liquid filledOralRedpharm Drug67296-2207
BenzonatateBenzonatate 100 mg/1Capsule, Liquid filledOralHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.23155-898
BenzonatateBenzonatate 200 mg/1Capsule, Liquid filledOralHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.23155-899
BenzonatateBenzonatate 100 mg/1Capsule, Liquid filledOralProficient Rx LP63187-076
BenzonatateBenzonatate 200 mg/1CapsuleOralChartwell RX, LLC62135-441
BenzonatateBenzonatate 100 mg/1CapsuleOralChartwell RX, LLC62135-440
BenzonatateBenzonatate 200 mg/1CapsuleOralBryant Ranch Prepack71335-2021

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