NDC codes

FDA NDC Directory
Product NDC (as listed)67296-2153Labeler and product segments. Claims need a package NDC.
Product NDC at billing width67296-2153Add 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
67296-2153-16729621530115 CAPSULE in 1 BOTTLE (67296-2153-1)Marketed from Apr 9, 2007
67296-2153-36729621530330 CAPSULE in 1 BOTTLE (67296-2153-3)Marketed from Apr 9, 2007

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
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 040597
Marketing start
Listing expires
Other FDA classes
Decreased Tracheobronchial Stretch Receptor Activity (Physiologic effect)
Identifiers
Product ID 67296-2153_4637e41d-954c-01cc-e063-6394a90a9ef9SPL ID 4637e41d-954c-01cc-e063-6394a90a9ef9SPL set ID 32524a8a-4cee-26c0-e063-6294a90aa898RxCUI 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

N467296215301 followed by a unit qualifier and the quantity

Package 67296-2153-01. 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 capsules are 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 040597

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

FDA NDC Directory listings under ANDA 040597
ProductStrengthForm · routeLabelerProduct NDC
BenzonatateBenzonatate 100 mg/1CapsuleOralAmerican Health Packaging68084-214
BenzonatateBenzonatate 100 mg/1Capsule, Liquid filledOralMajor Pharmaceuticals0904-6564
BenzonatateBenzonatate 100 mg/1CapsuleOralA-S Medication Solutions50090-6387
BenzonatateBenzonatate 200 mg/1CapsuleOralZydus Lifesciences Limited65841-843
BenzonatateBenzonatate 100 mg/1CapsuleOralDIRECT RX61919-400
BenzonatateBenzonatate 100 mg/1CapsuleOralA-S Medication Solutions50090-6850
BenzonatateBenzonatate 100 mg/1CapsuleOralProficient Rx LP63187-799
BenzonatateBenzonatate 200 mg/1Capsule, Liquid filledOralZydus Pharmaceuticals USA Inc.68382-091
BenzonatateBenzonatate 100 mg/1CapsuleOralBryant Ranch Prepack71335-0091
BenzonatateBenzonatate 200 mg/1CapsuleOralBryant Ranch Prepack71335-2790
BenzonatateBenzonatate 100 mg/1Capsule, Liquid filledOralZydus Pharmaceuticals USA Inc.68382-247
BenzonatateBenzonatate 200 mg/1CapsuleOralPreferred Pharmaceuticals Inc.68788-8405
BenzonatateBenzonatate 100 mg/1CapsuleOralZydus Lifesciences Limited65841-614
BenzonatateBenzonatate 200 mg/1CapsuleOralBryant Ranch Prepack71335-2590

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