Gabapentin NDC 70518-4532

NDC codes

FDA NDC Directory

Product NDC (as listed)70518-4532Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70518-4532Add 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
70518-4532-0	70518453200	100 POUCH in 1 BOX (70518-4532-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-4532-1)Marketed from Dec 7, 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): Gabapentin
Generic name (nonproprietary): gabapentin
Active ingredients: Gabapentin — 600 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: REMEDYREPACK INC.
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 217116
Marketing start: Dec 7, 2025
Listing expires: Dec 31, 2027
Other FDA classes: Decreased Central Nervous System Disorganized Electrical Activity (Physiologic effect)
Identifiers: Product ID 70518-4532_5b9b06b9-d8c4-4c21-e063-6294a90a9461SPL ID 5b9b06b9-d8c4-4c21-e063-6294a90a9461

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

N470518453200 followed by a unit qualifier and the quantity

Package 70518-4532-00. 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 217116

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

FDA NDC Directory listings under ANDA 217116
Product	Strength	Form · route	Labeler	Product NDC
Gabapentin	Gabapentin 600 mg/1	Tablet, Film coatedOral	Granules Pharmaceuticals Inc.	70010-227
Gabapentin	Gabapentin 800 mg/1	Tablet, Film coatedOral	Granules Pharmaceuticals Inc.	70010-228