NDC codes

FDA NDC Directory
Product NDC (as listed)58118-2126Labeler and product segments. Claims need a package NDC.
Product NDC at billing width58118-2126Add 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
58118-2126-8581182126085811821260830 TABLET in 1 BLISTER PACK (58118-2126-8)Marketed from Sep 9, 2026

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
Route
Oral
Labeler
Clinical Solutions Wholesale, LLCNDC labeler code 58118
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 077662
Marketing start
Listing expires
Other FDA classes
Decreased Central Nervous System Disorganized Electrical Activity (Physiologic effect)
Identifiers
Product ID 58118-2126_5b0eaffd-fce9-0548-e063-6394a90a4045SPL ID 5b0eaffd-fce9-0548-e063-6394a90a4045SPL set ID b7f9a106-52c6-49e4-acf5-8fb07761ba4fRxCUI 310433, 310434UNII 6CW7F3G59XUPC 0358118212786, 0358118212687

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

N458118212608 followed by a unit qualifier and the quantity

Package 58118-2126-08. 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)

Gabapentin tablets are indicated for: Management of postherpetic neuralgia in adults Adjunctive therapy in the treatment of partial onset seizures, with and without secondary generalization, in adults and pediatric patients 3 years and older with epilepsy Gabapentin tablets are indicated for: Postherpetic neuralgia in adults ( 1 ) Adjunctive therapy in the treatment of partial onset seizures, with and without secondary generalization, in adults and pediatric patients 3 years and older with epilepsy ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 58118-2126

What is NDC 58118-2126?
58118-2126 is the product NDC for Gabapentin, Gabapentin 600 mg/1 tablet, listed with the FDA by Clinical Solutions Wholesale, LLC. 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?
Clinical Solutions Wholesale, LLC, NDC labeler code 58118. 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 800 mg/1TabletOralSt. Mary's Medical Park Pharmacy60760-94360760-0943-3060760-0943-90
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

All 562 Gabapentin NDCs

Other NDCs under ANDA 077662

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

FDA NDC Directory listings under ANDA 077662
ProductStrengthForm · routeLabelerProduct NDC
GabapentinGabapentin 600 mg/1TabletOralBryant Ranch Prepack63629-7307
GabapentinGabapentin 800 mg/1TabletOralProficient Rx LP63187-010
GabapentinGabapentin 800 mg/1TabletOralBryant Ranch Prepack63629-7308
GabapentinGabapentin 800 mg/1TabletOralClinical Solutions Wholesale, LLC58118-2127
GabapentinGabapentin 600 mg/1TabletOralProficient Rx LP63187-057
GabapentinGabapentin 600 mg/1TabletOralCoupler LLC67046-1086
GabapentinGabapentin 600 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.55289-959
GabapentinGabapentin 600 mg/1TabletOralBluePoint Laboratories68001-411
GabapentinGabapentin 600 mg/1TabletOralBryant Ranch Prepack63629-3063
GabapentinGabapentin 800 mg/1TabletOralBluePoint Laboratories68001-412
GabapentinGabapentin 600 mg/1TabletOralUnit Dose Solutions, Inc.87441-036
GabapentinGabapentin 800 mg/1TabletOralBryant Ranch Prepack71335-0254
GabapentinGabapentin 800 mg/1TabletOralGlenmark Pharmaceuticals Inc., USA68462-127
GabapentinGabapentin 600 mg/1TabletOralGlenmark Pharmaceuticals Inc., USA68462-126

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