NDC codes

FDA NDC Directory
Product NDC (as listed)72789-232Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72789-0232Add 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
72789-232-21727890232217278902322121 CAPSULE in 1 BOTTLE, PLASTIC (72789-232-21)Marketed from May 9, 2022
72789-232-30727890232307278902323030 CAPSULE in 1 BOTTLE, PLASTIC (72789-232-30)Marketed from Feb 8, 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
Benzonatate — 200 mg/1
Dosage form
Capsule
Route
Oral
Labeler
PD-Rx Pharmaceuticals, Inc.NDC labeler code 72789
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 72789-232_5b7514eb-5e93-f9e1-e063-6294a90ad37bSPL ID 5b7514eb-5e93-f9e1-e063-6294a90ad37b
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

N472789023221 followed by a unit qualifier and the quantity

Package 72789-0232-21. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 72789-232

What is NDC 72789-232?
72789-232 is the product NDC for Benzonatate, Benzonatate 200 mg/1 capsule, listed with the FDA by PD-Rx Pharmaceuticals, Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Benzonatate.
What is the active ingredient?
Benzonatate.
Who is the labeler?
PD-Rx Pharmaceuticals, Inc., NDC labeler code 72789. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Benzonatate?
134 other product NDCs are listed under this name. See all Benzonatate NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Benzonatate NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
BenzonatateBenzonatate 100 mg/1CapsuleOralStrides Pharma Science Limited64380-71264380-0712-0664380-0712-07
BenzonatateBenzonatate 200 mg/1CapsuleOralStrides Pharma Science Limited64380-71364380-0713-0664380-0713-07
BenzonatateBenzonatate 150 mg/1CapsuleOralAnvi Pharmaceuticals Inc87519-11187519-0111-90
BenzonatateBenzonatate 100 mg/1CapsuleOralREMEDYREPACK INC.70518-455870518-4558-0070518-4558-0170518-4558-02+1 more
BenzonatateBenzonatate 100 mg/1CapsuleOralCoupler LLC67046-162967046-1629-03
BenzonatateBenzonatate 200 mg/1CapsuleOralREMEDYREPACK INC.70518-449770518-4497-0070518-4497-01
BenzonatateBenzonatate 100 mg/1CapsuleOralSt. Mary's Medical Park Pharmacy60760-86960760-0869-1560760-0869-30
BenzonatateBenzonatate 100 mg/1CapsuleOralCoupler LLC67046-148467046-1484-03
BenzonatateBenzonatate 200 mg/1CapsuleOralDirect_rx72189-60672189-0606-2072189-0606-30
BenzonatateBenzonatate 100 mg/1Capsule, Liquid filledOralHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.23155-89823155-0898-0123155-0898-05

All 135 Benzonatate NDCs

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 100 mg/1CapsuleOralMajor Pharmaceuticals0904-7153
BenzonatateBenzonatate 200 mg/1CapsuleOralQPharma Inc42708-171
BenzonatateBenzonatate 100 mg/1CapsuleOralEpic Pharma LLC42806-714
BenzonatateBenzonatate 200 mg/1CapsuleOralEpic Pharma LLC42806-715
BenzonatateBenzonatate 100 mg/1CapsuleOralA-S Medication Solutions50090-5409
BenzonatateBenzonatate 100 mg/1CapsuleOralA-S Medication Solutions50090-5986
BenzonatateBenzonatate 200 mg/1CapsuleOralA-S Medication Solutions50090-6294
BenzonatateBenzonatate 100 mg/1CapsuleOralNorthwind Health Company, LLC51655-754
BenzonatateBenzonatate 200 mg/1CapsuleOralNorthwind Health Company, LLC51655-762
BenzonatateBenzonatate 100 mg/1CapsuleOralCardinal Health 107, LLC55154-3372
BenzonatateBenzonatate 100 mg/1CapsuleOralSt. Mary's Medical Park Pharmacy60760-700
BenzonatateBenzonatate 200 mg/1CapsuleOralRedPharm Drug, Inc.67296-1751
BenzonatateBenzonatate 200 mg/1CapsuleOralNuCare Pharmaceuticals,Inc.68071-1395
BenzonatateBenzonatate 100 mg/1CapsuleOralNuCare Pharmaceuticals,Inc.68071-5083
BenzonatateBenzonatate 100 mg/1CapsuleOralNuCare Pharmaceuticals,Inc.68071-5223
BenzonatateBenzonatate 100 mg/1CapsuleOralPreferred Pharmaceuticals Inc68788-7607
BenzonatateBenzonatate 200 mg/1CapsuleOralPreferred Pharmaceuticals Inc.68788-8329
BenzonatateBenzonatate 200 mg/1CapsuleOralREMEDYREPACK INC.70518-2491
BenzonatateBenzonatate 100 mg/1CapsuleOralREMEDYREPACK INC.70518-2873
BenzonatateBenzonatate 100 mg/1CapsuleOralProficient Rx LP71205-632

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