NDC codes

FDA NDC Directory
Product NDC (as listed)51655-762Labeler and product segments. Claims need a package NDC.
Product NDC at billing width51655-0762Add 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
51655-762-205165507622020 CAPSULE in 1 BOTTLE, PLASTIC (51655-762-20)Marketed from Jul 16, 2021
51655-762-525165507625230 CAPSULE in 1 BOTTLE, PLASTIC (51655-762-52)Marketed from Sep 29, 2022

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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 206948
Marketing start
Listing expires
Other FDA classes
Decreased Tracheobronchial Stretch Receptor Activity (Physiologic effect)
Identifiers
Product ID 51655-762_4951a381-95f0-cd50-e063-6294a90a916eSPL ID 4951a381-95f0-cd50-e063-6294a90a916eSPL set ID da6cead3-2859-df03-e053-2a95a90a010bRxCUI 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

N451655076220 followed by a unit qualifier and the quantity

Package 51655-0762-20. 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, USP 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 206948

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

FDA NDC Directory listings under ANDA 206948
ProductStrengthForm · routeLabelerProduct NDC
BenzonatateBenzonatate 200 mg/1CapsuleOralQPharma Inc42708-171
BenzonatateBenzonatate 100 mg/1CapsuleOralCardinal Health 107, LLC55154-3372
BenzonatateBenzonatate 100 mg/1CapsuleOralNuCare Pharmaceuticals,Inc.68071-5083
BenzonatateBenzonatate 100 mg/1CapsuleOralSt. Mary's Medical Park Pharmacy60760-700
BenzonatateBenzonatate 100 mg/1CapsuleOralProficient Rx LP71205-632
BenzonatateBenzonatate 100 mg/1CapsuleOralA-S Medication Solutions50090-5986
BenzonatateBenzonatate 100 mg/1CapsuleOralEpic Pharma LLC42806-714
BenzonatateBenzonatate 200 mg/1CapsuleOralEpic Pharma LLC42806-715
BenzonatateBenzonatate 100 mg/1CapsuleOralNuCare Pharmaceuticals,Inc.68071-5223
BenzonatateBenzonatate 100 mg/1CapsuleOralDIRECT RX72189-194
BenzonatateBenzonatate 200 mg/1CapsuleOralDIRECT RX72189-192
BenzonatateBenzonatate 100 mg/1CapsuleOralSportpharm LLC85766-089
BenzonatateBenzonatate 100 mg/1CapsuleOralBryant Ranch Prepack71335-1544
BenzonatateBenzonatate 200 mg/1CapsuleOralSportpharm LLC85766-090
BenzonatateBenzonatate 200 mg/1CapsuleOralBryant Ranch Prepack71335-1553
BenzonatateBenzonatate 100 mg/1CapsuleOralPreferred Pharmaceuticals Inc68788-7607
BenzonatateBenzonatate 200 mg/1CapsuleOralREMEDYREPACK INC.70518-2491
BenzonatateBenzonatate 100 mg/1CapsuleOralAsclemed USA, Inc.76420-803
BenzonatateBenzonatate 200 mg/1CapsuleOralProficient Rx LP71205-643
BenzonatateBenzonatate 100 mg/1CapsuleOralA-S Medication Solutions50090-5409

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