What is NDC 60687-518?

60687-518 is the product NDC for Gabapentin, Gabapentin 800 mg/1 tablet, film coated, listed with the FDA by American Health Packaging. It has 1 package NDC, shown above in 10- and 11-digit form.

American Health Packaging, NDC labeler code 60687. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Gabapentin?

561 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Gabapentin NDC 60687-518 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)60687-518Labeler and product segments. Claims need a package NDC.

Product NDC at billing width60687-0518Add 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
60687-518-01	6068705180160687051801	100 BLISTER PACK in 1 CARTON (60687-518-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-518-11)Marketed from Mar 2, 2020

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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 — 800 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: American Health PackagingNDC labeler code 60687
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 078926
Marketing start: Mar 2, 2020
Listing expires: Dec 31, 2027
Other FDA classes: Decreased Central Nervous System Disorganized Electrical Activity (Physiologic effect)
Identifiers: Product ID 60687-518_5a5b753b-8c05-0390-e063-6394a90a0a50SPL ID 5a5b753b-8c05-0390-e063-6394a90a0a50

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

N460687051801 followed by a unit qualifier and the quantity

Package 60687-0518-01. 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.

About NDC 60687-518

What is NDC 60687-518?: 60687-518 is the product NDC for Gabapentin, Gabapentin 800 mg/1 tablet, film coated, listed with the FDA by American Health Packaging. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Gabapentin.
What is the active ingredient?: Gabapentin.
Who is the labeler?: American Health Packaging, NDC labeler code 60687. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Gabapentin?: 561 other product NDCs are listed under this name. See all Gabapentin 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 Gabapentin NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Gabapentin	Gabapentin 800 mg/1	TabletOral	St. Mary's Medical Park Pharmacy	60760-943	60760-0943-3060760-0943-90
gabapentin	Gabapentin 300 mg/1	CapsuleOral	REMEDYREPACK INC.	70518-4763	70518-4763-00
Gabapentin	Gabapentin 100 mg/1	CapsuleOral	Cardinal Health 107, LLC	55154-0581	55154-0581-00
Gabapentin	Gabapentin 100 mg/1	CapsuleOral	Advanced Rx of Tennessee, LLC	80425-0595	80425-0595-0180425-0595-0280425-0595-03+1 more
Gabapentin	Gabapentin 300 mg/1	CapsuleOral	REMEDYREPACK INC.	70518-4746	70518-4746-0070518-4746-0170518-4746-02+1 more
Gabapentin	Gabapentin 100 mg/1	CapsuleOral	REMEDYREPACK INC.	70518-4742	70518-4742-0070518-4742-02
Gabapentin	Gabapentin 400 mg/1	CapsuleOral	REMEDYREPACK INC.	70518-4740	70518-4740-0070518-4740-01
Gabapentin	Gabapentin 300 mg/1	CapsuleOral	Cardinal Health 107, LLC	55154-0580	55154-0580-00
Gabapentin	Gabapentin 600 mg/1	Tablet, CoatedOral	Coupler LLC	67046-1233	67046-1233-03
Gabapentin	Gabapentin 200 mg/1	CapsuleOral	Trifluent Pharma, LLC	73352-231	73352-0231-01

All 562 Gabapentin NDCs

Other NDCs under ANDA 078926

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

FDA NDC Directory listings under ANDA 078926
Product	Strength	Form · route	Labeler	Product NDC
Gabapentin	Gabapentin 800 mg/1	Tablet, Film coatedOral	PD-Rx Pharmaceuticals, Inc.	43063-611
Gabapentin	Gabapentin 600 mg/1	Tablet, Film coatedOral	Cardinal Health 107, LLC	55154-8189
Gabapentin	Gabapentin 800 mg/1	Tablet, Film coatedOral	Cardinal Health 107, LLC	55154-8193
Gabapentin	Gabapentin 600 mg/1	Tablet, Film coatedOral	American Health Packaging	60687-507
Gabapentin	Gabapentin 600 mg/1	Tablet, Film coatedOral	Zydus Lifesciences Limited	65841-705
Gabapentin	Gabapentin 800 mg/1	Tablet, Film coatedOral	Zydus Lifesciences Limited	65841-706
Gabapentin	Gabapentin 600 mg/1	Tablet, Film coatedOral	Zydus Pharmaceuticals USA Inc.	68382-204
Gabapentin	Gabapentin 800 mg/1	Tablet, Film coatedOral	Zydus Pharmaceuticals USA Inc.	68382-205
Gabapentin	Gabapentin 600 mg/1	Tablet, Film coatedOral	PD-Rx Pharmaceuticals, Inc.	72789-127