NDC codes

FDA NDC Directory
Product NDC (as listed)68071-3527Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68071-3527Add 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
68071-3527-36807135270330 CAPSULE in 1 BOTTLE, PLASTIC (68071-3527-3)Marketed from Nov 1, 2023
68071-3527-66807135270660 CAPSULE in 1 BOTTLE, PLASTIC (68071-3527-6)Marketed from Nov 1, 2023
68071-3527-96807135270990 CAPSULE in 1 BOTTLE, PLASTIC (68071-3527-9)Marketed from Nov 1, 2023

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 — 300 mg/1
Dosage form
Capsule
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 075477
Marketing start
Listing expires
Other FDA classes
Decreased Central Nervous System Disorganized Electrical Activity (Physiologic effect)
Identifiers
Product ID 68071-3527_2d3f8d53-7483-27fd-e063-6294a90a2171SPL ID 2d3f8d53-7483-27fd-e063-6294a90a2171SPL set ID 0919fed8-e968-b5ac-e063-6294a90afbffRxCUI 310431UNII 6CW7F3G59XUPC 0368071352795

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

N468071352703 followed by a unit qualifier and the quantity

Package 68071-3527-03. 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 is 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 is 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 075477

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

FDA NDC Directory listings under ANDA 075477
ProductStrengthForm · routeLabelerProduct NDC
GabapentinGabapentin 400 mg/1CapsuleOralMullan Pharmaceutical Inc.83301-0005
GabapentinGabapentin 300 mg/1CapsuleOralWestminster Pharmaceuticals, LLC69367-344
GabapentinGabapentin 300 mg/1CapsuleOralAdvanced Rx Pharmacy of Tennessee, LLC80425-0196
GabapentinGabapentin 100 mg/1CapsuleOralWestminster Pharmaceuticals, LLC69367-343
GabapentinGabapentin 400 mg/1CapsuleOralWestminster Pharmaceuticals, LLC69367-345
GabapentinGabapentin 100 mg/1CapsuleOralAdvanced Rx Pharmacy of Tennessee, LLC80425-0199
GabapentinGabapentin 400 mg/1CapsuleOralAdvanced Rx Pharmacy of Tennessee, LLC80425-0286
GabapentinGabapentin 300 mg/1CapsuleOralProficient Rx LP82804-217
GabapentinGabapentin 300 mg/1CapsuleOralMullan Pharmaceutical Inc.83301-0004
GabapentinGabapentin 100 mg/1CapsuleOralMullan Pharmaceutical Inc.83301-0003
GabapentinGabapentin 100 mg/1CapsuleOralProficient Rx LP82804-226

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