NDC codes

FDA NDC Directory
Product NDC (as listed)68462-127Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68462-0127Add 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
68462-127-0168462012701100 TABLET in 1 BOTTLE (68462-127-01)Marketed from Apr 1, 2006
68462-127-0568462012705500 TABLET in 1 BOTTLE (68462-127-05)Marketed from Apr 1, 2006

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
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 68462-127_4da1bae0-701b-4b65-a01e-f4bcedfad849SPL ID 4da1bae0-701b-4b65-a01e-f4bcedfad849SPL set ID 3865a6e3-112c-490c-82ac-35401336b16eRxCUI 310433, 310434UNII 6CW7F3G59XUPC 0368462127018, 0368462126011

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

N468462012701 followed by a unit qualifier and the quantity

Package 68462-0127-01. 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

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)

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/1TabletOralBluePoint Laboratories68001-411
GabapentinGabapentin 800 mg/1TabletOralBluePoint Laboratories68001-412
GabapentinGabapentin 800 mg/1TabletOralBryant Ranch Prepack71335-0254
GabapentinGabapentin 600 mg/1TabletOralBryant Ranch Prepack63629-3063
GabapentinGabapentin 600 mg/1TabletOralUnit Dose Solutions, Inc.87441-036
GabapentinGabapentin 600 mg/1TabletOralGlenmark Pharmaceuticals Inc., USA68462-126
GabapentinGabapentin 800 mg/1TabletOralProficient Rx LP63187-010
GabapentinGabapentin 600 mg/1TabletOralClinical Solutions Wholesale, LLC58118-2126
GabapentinGabapentin 600 mg/1TabletOralBryant Ranch Prepack63629-7307
GabapentinGabapentin 800 mg/1TabletOralClinical Solutions Wholesale, LLC58118-2127
GabapentinGabapentin 800 mg/1TabletOralBryant Ranch Prepack63629-7308
GabapentinGabapentin 600 mg/1TabletOralProficient Rx LP63187-057
GabapentinGabapentin 600 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.55289-959
GabapentinGabapentin 600 mg/1TabletOralCoupler LLC67046-1086

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