NDC codes

FDA NDC Directory
Product NDC (as listed)60760-943Labeler and product segments. Claims need a package NDC.
Product NDC at billing width60760-0943Add 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
60760-943-30607600943306076009433030 TABLET in 1 BOTTLE, PLASTIC (60760-943-30)Marketed from Oct 14, 2026
60760-943-90607600943906076009439090 TABLET in 1 BOTTLE, PLASTIC (60760-943-90)Marketed from Oct 14, 2026

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
Route
Oral
Labeler
St. Mary's Medical Park PharmacyNDC labeler code 60760
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 203244
Marketing start
Listing expires
Other FDA classes
Decreased Central Nervous System Disorganized Electrical Activity (Physiologic effect)
Identifiers
Product ID 60760-943_5de61c29-06e3-b9e5-e063-6294a90a4b29SPL ID 5de61c29-06e3-b9e5-e063-6294a90a4b29

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

N460760094330 followed by a unit qualifier and the quantity

Package 60760-0943-30. 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 60760-943

What is NDC 60760-943?
60760-943 is the product NDC for Gabapentin, Gabapentin 800 mg/1 tablet, listed with the FDA by St. Mary's Medical Park Pharmacy. It has 2 package NDCs, 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?
St. Mary's Medical Park Pharmacy, NDC labeler code 60760. 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
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
gabapentinGabapentin 300 mg/1CapsuleOralREMEDYREPACK INC.70518-476370518-4763-00
GabapentinGabapentin 100 mg/1CapsuleOralCardinal Health 107, LLC55154-058155154-0581-00
GabapentinGabapentin 100 mg/1CapsuleOralAdvanced Rx of Tennessee, LLC80425-059580425-0595-0180425-0595-0280425-0595-03+1 more
GabapentinGabapentin 300 mg/1CapsuleOralREMEDYREPACK INC.70518-474670518-4746-0070518-4746-0170518-4746-02+1 more
GabapentinGabapentin 100 mg/1CapsuleOralREMEDYREPACK INC.70518-474270518-4742-0070518-4742-02
GabapentinGabapentin 400 mg/1CapsuleOralREMEDYREPACK INC.70518-474070518-4740-00
GabapentinGabapentin 300 mg/1CapsuleOralCardinal Health 107, LLC55154-058055154-0580-00
GabapentinGabapentin 600 mg/1Tablet, CoatedOralCoupler LLC67046-123367046-1233-03
GabapentinGabapentin 200 mg/1CapsuleOralTrifluent Pharma, LLC73352-23173352-0231-01
GabapentinGabapentin 600 mg/1TabletOralCoupler LLC67046-108667046-1086-03

All 562 Gabapentin NDCs

Other NDCs under ANDA 203244

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

FDA NDC Directory listings under ANDA 203244
ProductStrengthForm · routeLabelerProduct NDC
GabapentinGabapentin 600 mg/1Tablet, Film coatedOralSt. Mary's Medical Park Pharmacy60760-066
GabapentinGabapentin 600 mg/1TabletOralStrides Pharma Science Limited64380-727
GabapentinGabapentin 800 mg/1TabletOralStrides Pharma Science Limited64380-728
GabapentinGabapentin 800 mg/1Tablet, Film coatedOralProficient Rx LP71205-160
GabapentinGabapentin 600 mg/1Tablet, Film coatedOralProficient Rx LP71205-457
GabapentinGabapentin 800 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-1007
GabapentinGabapentin 600 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-1026
GabapentinGabapentin 800 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-1041
GabapentinGabapentin 600 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-1132
GabapentinGabapentin 800 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-1601
GabapentinGabapentin 600 mg/1Tablet, Film coatedOralAphena Pharma Solutions - Tennessee, LLC71610-044
GabapentinGabapentin 800 mg/1Tablet, Film coatedOralAphena Pharma Solutions - Tennessee, LLC71610-426
GabapentinGabapentin 600 mg/1Tablet, Film coatedOralBryant Ranch Prepack72162-2141
GabapentinGabapentin 800 mg/1Tablet, Film coatedOralBryant Ranch Prepack72162-2142
GabapentinGabapentin 800 mg/1Tablet, Film coatedOralDIRECT RX72189-158

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