NDC codes

FDA NDC Directory
Product NDC (as listed)69452-144Labeler and product segments. Claims need a package NDC.
Product NDC at billing width69452-0144Add 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
69452-144-206945201442069452014420100 CAPSULE in 1 BOTTLE, PLASTIC (69452-144-20)Marketed from Aug 15, 2016
69452-144-306945201443069452014430500 CAPSULE in 1 BOTTLE, PLASTIC (69452-144-30)Marketed from Aug 15, 2016

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
Bionpharma Inc.NDC labeler code 69452
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 081297
Marketing start
Listing expires
Other FDA classes
Decreased Tracheobronchial Stretch Receptor Activity (Physiologic effect)
Identifiers
Product ID 69452-144_54f1a3e7-6d29-ac5e-e063-6394a90ad5b5SPL ID 54f1a3e7-6d29-ac5e-e063-6394a90ad5b5SPL set ID 2630be01-1d2d-4c40-8e56-8568ea89eacfRxCUI 197397, 283417UNII 5P4DHS6ENRUPC 0369452143209
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

N469452014420 followed by a unit qualifier and the quantity

Package 69452-0144-20. 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 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)

About NDC 69452-144

What is NDC 69452-144?
69452-144 is the product NDC for Benzonatate, Benzonatate 200 mg/1 capsule, listed with the FDA by Bionpharma 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?
Bionpharma Inc., NDC labeler code 69452. 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 081297

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

FDA NDC Directory listings under ANDA 081297
ProductStrengthForm · routeLabelerProduct NDC
BenzonatateBenzonatate 200 mg/1CapsuleOralGolden State Medical Supply, Inc.60429-914
BenzonatateBenzonatate 100 mg/1CapsuleOralGolden State Medical Supply, Inc.60429-927
BenzonatateBenzonatate 100 mg/1CapsuleOralCoupler LLC67046-1484
BenzonatateBenzonatate 100 mg/1CapsuleOralNuCare Pharmaceuticals,Inc.68071-5105
BenzonatateBenzonatate 100 mg/1CapsuleOralNuCare Pharmaceuticals,Inc.68071-5156
BenzonatateBenzonatate 100 mg/1CapsuleOralBionpharma Inc.69452-143
BenzonatateBenzonatate 100 mg/1CapsuleOralProficient Rx LP71205-067
BenzonatateBenzonatate 200 mg/1CapsuleOralProficient Rx LP71205-605
BenzonatateBenzonatate 200 mg/1CapsuleOralBryant Ranch Prepack71335-1880
BenzonatateBenzonatate 100 mg/1CapsuleOralBryant Ranch Prepack71335-1927
BenzonatateBenzonatate 100 mg/1CapsuleOralAphena Pharma Solutions - Tennessee, LLC71610-692

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