NDC codes

FDA NDC Directory
Product NDC (as listed)50268-325Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50268-0325Add 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
50268-325-155026803251550 BLISTER PACK in 1 BOX (50268-325-15) / 1 TABLET, COATED in 1 BLISTER PACK (50268-325-11)Marketed from May 1, 2023

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 — 600 mg/1
Dosage form
Tablet, Coated
Route
Oral
Labeler
AvPAK
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 207057
Marketing start
Listing expires
Other FDA classes
Decreased Central Nervous System Disorganized Electrical Activity (Physiologic effect)
Identifiers
Product ID 50268-325_2b4c1c97-dc71-3801-e063-6394a90a7fafSPL ID 2b4c1c97-dc71-3801-e063-6394a90a7fafSPL set ID faa47fcd-2545-a946-e053-6294a90a05d2RxCUI 310433UNII 6CW7F3G59X

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

N450268032515 followed by a unit qualifier and the quantity

Package 50268-0325-15. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 207057

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

FDA NDC Directory listings under ANDA 207057
ProductStrengthForm · routeLabelerProduct NDC
GabapentinGabapentin 800 mg/1Tablet, CoatedOralWestminster Pharmaceuticals, LLC69367-347
GabapentinGabapentin 600 mg/1Tablet, CoatedOralWestminster Pharmaceuticals, LLC69367-346
GabapentinGabapentin 800 mg/1Tablet, CoatedOralMullan Pharmaceutical Inc.83301-0002
GabapentinGabapentin 600 mg/1Tablet, CoatedOralMullan Pharmaceutical Inc.83301-0001
GabapentinGabapentin 600 mg/1Tablet, CoatedOralAdvanced Rx of Tennessee, LLC80425-0201
GabapentinGabapentin 800 mg/1Tablet, CoatedOralAdvanced Rx of Tennessee, LLC80425-0204
GabapentinGabapentin 800 mg/1Tablet, CoatedOralA-S Medication Solutions50090-7400
GabapentinGabapentin 800 mg/1Tablet, CoatedOralProficient Rx LP82804-203
GabapentinGabapentin 600 mg/1Tablet, CoatedOralProficient Rx LP82804-210
GabapentinGabapentin 600 mg/1Tablet, CoatedOralTAGI Pharma, Inc.51224-021
GabapentinGabapentin 800 mg/1Tablet, CoatedOralTAGI Pharma, Inc.51224-121
GabapentinGabapentin 800 mg/1Tablet, CoatedOralNuCare Pharmaceuticals,Inc.68071-3523
GabapentinGabapentin 600 mg/1Tablet, CoatedOralA-S Medication Solutions50090-7268
GabapentinGabapentin 600 mg/1Tablet, CoatedOralPrecision Dose, Inc.68094-069
GabapentinGabapentin 600 mg/1Tablet, CoatedOralNuCare Pharmaceuticals, Inc.68071-3783
GabapentinGabapentin 600 mg/1Tablet, CoatedOralA-S Medication Solutions50090-7269
GabapentinGabapentin 600 mg/1Tablet, CoatedOralCoupler LLC67046-1233
GabapentinGabapentin 800 mg/1Tablet, CoatedOralPrecision Dose, Inc.68094-489
GabapentinGabapentin 600 mg/1Tablet, CoatedOralBryant Ranch Prepack71335-1287
GabapentinGabapentin 600 mg/1Tablet, CoatedOralPrecision Dose, Inc.68094-589

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