NDC codes

FDA NDC Directory
Product NDC (as listed)63629-2476Labeler and product segments. Claims need a package NDC.
Product NDC at billing width63629-2476Add 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
63629-2476-163629247601100 CAPSULE in 1 BOTTLE (63629-2476-1)Marketed from Aug 10, 2015

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
Benzonatate — 200 mg/1
Dosage form
Capsule
Route
Oral
Labeler
Bryant Ranch PrepackNDC labeler code 63629
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 202765
Marketing start
Listing expires
Other FDA classes
Decreased Tracheobronchial Stretch Receptor Activity (Physiologic effect)
Identifiers
Product ID 63629-2476_6ad351a4-5f72-43d5-bc22-6eea86c0896eSPL ID 6ad351a4-5f72-43d5-bc22-6eea86c0896eSPL set ID 2471d5d9-ea9e-482a-811d-ad173b253be7RxCUI 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

N463629247601 followed by a unit qualifier and the quantity

Package 63629-2476-01. 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 Capsule 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 63629-2476

What is NDC 63629-2476?
63629-2476 is the product NDC for Benzonatate, Benzonatate 200 mg/1 capsule, listed with the FDA by Bryant Ranch Prepack. It has 1 package NDC, 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?
Bryant Ranch Prepack, NDC labeler code 63629. 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?
135 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 136 Benzonatate NDCs

Other NDCs under ANDA 202765

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

FDA NDC Directory listings under ANDA 202765
ProductStrengthForm · routeLabelerProduct NDC
BenzonatateBenzonatate 200 mg/1CapsuleOralProficient Rx LP63187-606
BenzonatateBenzonatate 200 mg/1CapsuleOralBryant Ranch Prepack63629-2475
BenzonatateBenzonatate 100 mg/1CapsuleOralPrecision Dose, Inc.68094-798
BenzonatateBenzonatate 100 mg/1CapsuleOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8661
BenzonatateBenzonatate 200 mg/1CapsuleOralPrecision Dose, Inc.68094-901
BenzonatateBenzonatate 200 mg/1CapsuleOralBryant Ranch Prepack71335-2853
BenzonatateBenzonatate 200 mg/1CapsuleOralREMEDYREPACK INC.70518-4497
BenzonatateBenzonatate 100 mg/1CapsuleOralRising Pharma Holdings, Inc.64980-634
BenzonatateBenzonatate 200 mg/1CapsuleOralRising Pharma Holdings, Inc.64980-635
BenzonatateBenzonatate 100 mg/1CapsuleOralBryant Ranch Prepack71335-2672
BenzonatateBenzonatate 100 mg/1CapsuleOralREMEDYREPACK INC.70518-4558
BenzonatateBenzonatate 100 mg/1CapsuleOralRedpharm Drug67296-2194
BenzonatateBenzonatate 200 mg/1CapsuleOralBryant Ranch Prepack71335-0031
BenzonatateBenzonatate 100 mg/1CapsuleOralBryant Ranch Prepack63629-9189
BenzonatateBenzonatate 200 mg/1CapsuleOralTAGI Pharma, Inc.51224-001
BenzonatateBenzonatate 100 mg/1CapsuleOralSt. Mary's Medical Park Pharmacy60760-869
BenzonatateBenzonatate 100 mg/1CapsuleOralTAGI Pharma, Inc.51224-010
BenzonatateBenzonatate 200 mg/1CapsuleOralRedpharm Drug67296-2244
BenzonatateBenzonatate 100 mg/1CapsuleOralBryant Ranch Prepack72162-1561
BenzonatateBenzonatate 200 mg/1CapsuleOralBryant Ranch Prepack72162-1560

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Benzonatate NDC 63629-2476 | National Drug Code | Med-Code