Benzonatate NDC 70518-4497

NDC codes

FDA NDC Directory

Product NDC (as listed)70518-4497Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70518-4497Add 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 NDC	11-digit (billing)	Package	Copy
70518-4497-0	70518449700	20 CAPSULE in 1 BOTTLE, PLASTIC (70518-4497-0)Marketed from Oct 10, 2025
70518-4497-1	70518449701	30 CAPSULE in 1 BOTTLE, PLASTIC (70518-4497-1)Marketed from Oct 16, 2025

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: REMEDYREPACK INC.
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 202765
Marketing start: Oct 10, 2025
Listing expires: Dec 31, 2027
Other FDA classes: Decreased Tracheobronchial Stretch Receptor Activity (Physiologic effect)
Identifiers: Product ID 70518-4497_5b74c5da-4c62-85f4-e063-6294a90a848bSPL ID 5b74c5da-4c62-85f4-e063-6294a90a848b
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

N470518449700 followed by a unit qualifier and the quantity

Package 70518-4497-00. 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

The FDA listing for this product does not reference a label (SPL) set.

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
Product	Strength	Form · route	Labeler	Product NDC
Benzonatate	Benzonatate 100 mg/1	CapsuleOral	Rising Pharma Holdings, Inc.	64980-634
Benzonatate	Benzonatate 200 mg/1	CapsuleOral	Rising Pharma Holdings, Inc.	64980-635
Benzonatate	Benzonatate 100 mg/1	CapsuleOral	Bryant Ranch Prepack	71335-2672
Benzonatate	Benzonatate 100 mg/1	CapsuleOral	NCS HealthCare of KY, LLC dba Vangard Labs	0615-8661
Benzonatate	Benzonatate 100 mg/1	CapsuleOral	Redpharm Drug	67296-2194
Benzonatate	Benzonatate 100 mg/1	CapsuleOral	REMEDYREPACK INC.	70518-4558
Benzonatate	Benzonatate 200 mg/1	CapsuleOral	TAGI Pharma, Inc.	51224-001
Benzonatate	Benzonatate 100 mg/1	CapsuleOral	Bryant Ranch Prepack	63629-9189
Benzonatate	Benzonatate 100 mg/1	CapsuleOral	TAGI Pharma, Inc.	51224-010
Benzonatate	Benzonatate 100 mg/1	CapsuleOral	St. Mary's Medical Park Pharmacy	60760-869
Benzonatate	Benzonatate 200 mg/1	CapsuleOral	Bryant Ranch Prepack	71335-0031
Benzonatate	Benzonatate 200 mg/1	CapsuleOral	Redpharm Drug	67296-2244
Benzonatate	Benzonatate 200 mg/1	CapsuleOral	Bryant Ranch Prepack	72162-1560
Benzonatate	Benzonatate 100 mg/1	CapsuleOral	Bryant Ranch Prepack	72162-1561
Benzonatate	Benzonatate 100 mg/1	CapsuleOral	A-S Medication Solutions	50090-4969
Benzonatate	Benzonatate 100 mg/1	CapsuleOral	A-S Medication Solutions	50090-4968
Benzonatate	Benzonatate 100 mg/1	CapsuleOral	Bryant Ranch Prepack	71335-1968
Benzonatate	Benzonatate 100 mg/1	CapsuleOral	Bryant Ranch Prepack	63629-2474
Benzonatate	Benzonatate 100 mg/1	CapsuleOral	Bryant Ranch Prepack	63629-2473
Benzonatate	Benzonatate 200 mg/1	CapsuleOral	Bryant Ranch Prepack	63629-2475

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