NDC codes

FDA NDC Directory
Product NDC (as listed)72189-178Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72189-0178Add 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
72189-178-307218901783030 TABLET in 1 BOTTLE (72189-178-30)Marketed from Feb 8, 2021
72189-178-7272189017872120 TABLET in 1 BOTTLE (72189-178-72)Marketed from Feb 8, 2021
72189-178-907218901789090 TABLET in 1 BOTTLE (72189-178-90)Marketed from Feb 8, 2021

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
Labeler
DIRECT RXNDC labeler code 72189
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 205101
Marketing start
Listing expires
Other FDA classes
Decreased Central Nervous System Disorganized Electrical Activity (Physiologic effect)
Identifiers
Product ID 72189-178_2becf606-de3d-b686-e063-6294a90afe58SPL ID 2becf606-de3d-b686-e063-6294a90afe58SPL set ID a7e45e3f-e382-32ba-e053-2a95a90a2537RxCUI 310430, 310432, 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

N472189017830 followed by a unit qualifier and the quantity

Package 72189-0178-30. 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 .

Full label on DailyMed (opens in a new tab)

About NDC 72189-178

What is NDC 72189-178?
72189-178 is the product NDC for Gabapentin, Gabapentin 800 mg/1 tablet, listed with the FDA by DIRECT RX. It has 3 package NDCs, 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?
DIRECT RX, NDC labeler code 72189. 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 300 mg/1CapsuleOralREMEDYREPACK INC.70518-476370518-4763-00
GabapentinGabapentin 100 mg/1CapsuleOralAdvanced Rx of Tennessee, LLC80425-059580425-0595-0180425-0595-0280425-0595-03+1 more
GabapentinGabapentin 100 mg/1CapsuleOralCardinal Health 107, LLC55154-058155154-0581-00
GabapentinGabapentin 300 mg/1CapsuleOralREMEDYREPACK INC.70518-474670518-4746-0070518-4746-0170518-4746-02
GabapentinGabapentin 100 mg/1CapsuleOralREMEDYREPACK INC.70518-474270518-4742-00
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
GabapentinGabapentin 600 mg/1TabletOralCoupler LLC67046-108667046-1086-03

All 562 Gabapentin NDCs

Other NDCs under ANDA 205101

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

FDA NDC Directory listings under ANDA 205101
ProductStrengthForm · routeLabelerProduct NDC
GabapentinGabapentin 800 mg/1TabletOralAsclemed USA, Inc.76420-497
GabapentinGabapentin 600 mg/1TabletOralProficient Rx LP82804-015
GabapentinGabapentin 600 mg/1TabletOralBryant Ranch Prepack72162-1530
GabapentinGabapentin 600 mg/1TabletOralHAWAII REPACK, INC.85534-0009
GabapentinGabapentin 800 mg/1TabletOralHAWAII REPACK, INC.85534-0010
GabapentinGabapentin 800 mg/1TabletOralBryant Ranch Prepack72162-1531
GabapentinGabapentin 800 mg/1TabletOralPreferred Pharmaceuticals, Inc.68788-7757
GabapentinGabapentin 600 mg/1TabletOralRadha Pharmaceuticals, Inc.77771-177
GabapentinGabapentin 800 mg/1TabletOralRadha Pharmaceuticals, Inc.77771-178
GabapentinGabapentin 800 mg/1TabletOralPreferred Pharmaceuticals, Inc.68788-7774
GabapentinGabapentin 600 mg/1TabletOralCreekwood Pharmaceuticals LLC82619-145
GabapentinGabapentin 800 mg/1TabletOralCreekwood Pharmaceuticals LLC82619-146
GabapentinGabapentin 800 mg/1TabletOralProficient Rx LP71205-774
GabapentinGabapentin 800 mg/1TabletOralProficient Rx LP71205-514
GabapentinGabapentin 600 mg/1TabletOralDirectrx72189-313
GabapentinGabapentin 600 mg/1TabletOralAsclemed USA, Inc.76420-235
GabapentinGabapentin 600 mg/1TabletOralProficient Rx LP71205-533
GabapentinGabapentin 800 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-217
GabapentinGabapentin 800 mg/1TabletOralSt. Mary's Medical Park Pharmacy60760-517
GabapentinGabapentin 800 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-737

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