NDC codes

FDA NDC Directory
Product NDC (as listed)50090-6189Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50090-6189Add 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
50090-6189-05009061890060 TABLET in 1 BOTTLE (50090-6189-0)Marketed from Oct 27, 2022
50090-6189-15009061890190 TABLET in 1 BOTTLE (50090-6189-1)Marketed from Oct 27, 2022
50090-6189-25009061890230 TABLET in 1 BOTTLE (50090-6189-2)Marketed from Oct 27, 2022

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 — 800 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 214957
Marketing start
Listing expires
Other FDA classes
Decreased Central Nervous System Disorganized Electrical Activity (Physiologic effect)
Identifiers
Product ID 50090-6189_293a0007-ee4b-46b0-a69e-2ff3622ddcf3SPL ID 293a0007-ee4b-46b0-a69e-2ff3622ddcf3SPL set ID 40bb60c0-a2f3-4e7f-b13c-028c906c4852RxCUI 310434UNII 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

N450090618900 followed by a unit qualifier and the quantity

Package 50090-6189-00. 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 214957

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

FDA NDC Directory listings under ANDA 214957
ProductStrengthForm · routeLabelerProduct NDC
GabapentinGabapentin 800 mg/1TabletOralDirect_Rx72189-394
GabapentinGabapentin 600 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-8476
GabapentinGabapentin 600 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-8488
GabapentinGabapentin 800 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-8790
GabapentinGabapentin 600 mg/1TabletOralBryant Ranch Prepack71335-3143
GabapentinGabapentin 600 mg/1TabletOralCoupler LLC67046-1535
GabapentinGabapentin 600 mg/1TabletOralDirect_Rx72189-471
GabapentinGabapentin 600 mg/1TabletOralCamber Pharmaceuticals, Inc.31722-166
GabapentinGabapentin 800 mg/1TabletOralCamber Pharmaceuticals, Inc.31722-167
GabapentinGabapentin 600 mg/1TabletOralPHOENIX RX LLC85509-1166
GabapentinGabapentin 600 mg/1TabletOralProficient Rx LP82804-193
GabapentinGabapentin 600 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-621
GabapentinGabapentin 600 mg/1TabletOralClinical Solutions Wholesale, LLC58118-0166
GabapentinGabapentin 800 mg/1TabletOralST. MARY'S MEDICAL PARK PHARMACY60760-837
GabapentinGabapentin 800 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-630
GabapentinGabapentin 800 mg/1TabletOralProficient Rx LP82804-249
GabapentinGabapentin 800 mg/1TabletOralClinical Solutions Wholesale, LLC58118-1167
GabapentinGabapentin 600 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-3445
GabapentinGabapentin 600 mg/1TabletOralExelan Pharmaceuticals, Inc.76282-706
GabapentinGabapentin 800 mg/1TabletOralExelan Pharmaceuticals, Inc.76282-707

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