NDC codes

FDA NDC Directory
Product NDC (as listed)71335-0688Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-0688Add 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
71335-0688-0713350688007133506880010 CAPSULE in 1 BOTTLE (71335-0688-0)Marketed from May 28, 2026
71335-0688-1713350688017133506880130 CAPSULE in 1 BOTTLE (71335-0688-1)Marketed from May 28, 2026
71335-0688-2713350688027133506880220 CAPSULE in 1 BOTTLE (71335-0688-2)Marketed from May 28, 2026
71335-0688-37133506880371335068803100 CAPSULE in 1 BOTTLE (71335-0688-3)Marketed from May 28, 2026
71335-0688-4713350688047133506880415 CAPSULE in 1 BOTTLE (71335-0688-4)Marketed from May 28, 2026
71335-0688-57133506880571335068805120 CAPSULE in 1 BOTTLE (71335-0688-5)Marketed from May 28, 2026
71335-0688-6713350688067133506880660 CAPSULE in 1 BOTTLE (71335-0688-6)Marketed from May 28, 2026
71335-0688-7713350688077133506880790 CAPSULE in 1 BOTTLE (71335-0688-7)Marketed from May 28, 2026
71335-0688-8713350688087133506880814 CAPSULE in 1 BOTTLE (71335-0688-8)Marketed from May 28, 2026
71335-0688-9713350688097133506880940 CAPSULE in 1 BOTTLE (71335-0688-9)Marketed from May 28, 2026

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 — 100 mg/1
Dosage form
Capsule
Route
Oral
Labeler
Bryant Ranch PrepackNDC labeler code 71335
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 040627
Marketing start
Listing expires
Other FDA classes
Decreased Tracheobronchial Stretch Receptor Activity (Physiologic effect)
Identifiers
Product ID 71335-0688_7db8b947-2c4f-4ca8-867a-bebe58f2327bSPL ID 7db8b947-2c4f-4ca8-867a-bebe58f2327bSPL set ID a788cb01-6dc3-4f28-aaa0-c23ac058c39aRxCUI 197397, 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

N471335068800 followed by a unit qualifier and the quantity

Package 71335-0688-00. 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 USP 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 71335-0688

What is NDC 71335-0688?
71335-0688 is the product NDC for benzonatate, Benzonatate 100 mg/1 capsule, listed with the FDA by Bryant Ranch Prepack. It has 10 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?
Bryant Ranch Prepack, NDC labeler code 71335. 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 040627

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

FDA NDC Directory listings under ANDA 040627
ProductStrengthForm · routeLabelerProduct NDC
benzonatateBenzonatate 100 mg/1CapsuleOralBryant Ranch Prepack71335-1329
BenzonatateBenzonatate 200 mg/1CapsuleOralQPharma, Inc.42708-082
benzonatateBenzonatate 100 mg/1CapsuleOralProficient Rx LP71205-971
BenzonatateBenzonatate 100 mg/1CapsuleOralAscend Laboratories, LLC67877-573
BenzonatateBenzonatate 200 mg/1CapsuleOralAscend Laboratories, LLC67877-575
BenzonatateBenzonatate 200 mg/1CapsuleOralNorthwind Health Company, LLC51655-776
BenzonatateBenzonatate 100 mg/1CapsuleOralCoupler LLC67046-1629
benzonatateBenzonatate 100 mg/1CapsuleOralProficient Rx LP63187-928

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