NDC codes

FDA NDC Directory
Product NDC (as listed)71335-1329Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-1329Add 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
71335-1329-07133513290010 CAPSULE in 1 BOTTLE (71335-1329-0)Marketed from Mar 22, 2017
71335-1329-17133513290130 CAPSULE in 1 BOTTLE (71335-1329-1)Marketed from Mar 22, 2017
71335-1329-27133513290220 CAPSULE in 1 BOTTLE (71335-1329-2)Marketed from Mar 22, 2017
71335-1329-371335132903100 CAPSULE in 1 BOTTLE (71335-1329-3)Marketed from Mar 22, 2017
71335-1329-47133513290415 CAPSULE in 1 BOTTLE (71335-1329-4)Marketed from Mar 22, 2017
71335-1329-571335132905120 CAPSULE in 1 BOTTLE (71335-1329-5)Marketed from Mar 22, 2017
71335-1329-67133513290660 CAPSULE in 1 BOTTLE (71335-1329-6)Marketed from Mar 22, 2017
71335-1329-77133513290790 CAPSULE in 1 BOTTLE (71335-1329-7)Marketed from Mar 22, 2017
71335-1329-87133513290814 CAPSULE in 1 BOTTLE (71335-1329-8)Marketed from Mar 22, 2017
71335-1329-97133513290940 CAPSULE in 1 BOTTLE (71335-1329-9)Marketed from Mar 22, 2017

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
Benzonatate100 mg/1
Dosage form
Capsule
Route
Oral
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 71335-1329_2e12fdc7-0714-440e-b918-4a080745f10dSPL ID 2e12fdc7-0714-440e-b918-4a080745f10dSPL set ID 143a5ba8-0ee9-43be-a0da-2c455c1a46bdRxCUI 197397UNII 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

N471335132900 followed by a unit qualifier and the quantity

Package 71335-1329-00. 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)

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/1CapsuleOralProficient Rx LP71205-971
BenzonatateBenzonatate 100 mg/1CapsuleOralAscend Laboratories, LLC67877-573
BenzonatateBenzonatate 200 mg/1CapsuleOralAscend Laboratories, LLC67877-575
benzonatateBenzonatate 100 mg/1CapsuleOralBryant Ranch Prepack71335-0688
BenzonatateBenzonatate 200 mg/1CapsuleOralNorthwind Health Company, LLC51655-776
BenzonatateBenzonatate 100 mg/1CapsuleOralCoupler LLC67046-1629
BenzonatateBenzonatate 200 mg/1CapsuleOralQPharma, Inc.42708-082
benzonatateBenzonatate 100 mg/1CapsuleOralProficient Rx LP63187-928

Free account

Keep searching with a free account

You’ve used your 3 free searches for this session. Log in or create a free Med-Code account to keep looking up NDCs, J-codes and drugs.

Create a free accountLog in