NDC codes

FDA NDC Directory
Product NDC (as listed)68071-5105Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68071-5105Add 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
68071-5105-4680715105044 CAPSULE in 1 BOTTLE (68071-5105-4)Marketed from Nov 6, 2019

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
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 68071-5105_1b469ff6-52eb-a91b-e063-6394a90a3123SPL ID 1b469ff6-52eb-a91b-e063-6394a90a3123SPL set ID 96b260c3-e177-73c3-e053-2a95a90a775eRxCUI 197397UNII 5P4DHS6ENRUPC 0368071510546
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

N468071510504 followed by a unit qualifier and the quantity

Package 68071-5105-04. 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)

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/1CapsuleOralProficient Rx LP71205-605
BenzonatateBenzonatate 100 mg/1CapsuleOralCoupler LLC67046-1484
BenzonatateBenzonatate 100 mg/1CapsuleOralNuCare Pharmaceuticals,Inc.68071-5156
BenzonatateBenzonatate 100 mg/1CapsuleOralProficient Rx LP71205-067
BenzonatateBenzonatate 200 mg/1CapsuleOralBryant Ranch Prepack71335-1880
BenzonatateBenzonatate 200 mg/1CapsuleOralGolden State Medical Supply, Inc.60429-914
BenzonatateBenzonatate 100 mg/1CapsuleOralGolden State Medical Supply, Inc.60429-927
BenzonatateBenzonatate 100 mg/1CapsuleOralBryant Ranch Prepack71335-1927
BenzonatateBenzonatate 100 mg/1CapsuleOralBionpharma Inc.69452-143
BenzonatateBenzonatate 200 mg/1CapsuleOralBionpharma Inc.69452-144
BenzonatateBenzonatate 100 mg/1CapsuleOralAphena Pharma Solutions - Tennessee, LLC71610-692

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