NDC codes

FDA NDC Directory
Product NDC (as listed)82804-210Labeler and product segments. Claims need a package NDC.
Product NDC at billing width82804-0210Add 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
82804-210-30828040210308280402103030 TABLET, COATED in 1 BOTTLE, PLASTIC (82804-210-30)Marketed from Sep 9, 2026
82804-210-90828040210908280402109090 TABLET, COATED in 1 BOTTLE, PLASTIC (82804-210-90)Marketed from Mar 1, 2025

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
Proficient Rx LPNDC labeler code 82804
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 82804-210_017c9376-14aa-40b7-a651-eb5d95e8f1daSPL ID 017c9376-14aa-40b7-a651-eb5d95e8f1da

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

N482804021030 followed by a unit qualifier and the quantity

Package 82804-0210-30. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 82804-210

What is NDC 82804-210?
82804-210 is the product NDC for Gabapentin, Gabapentin 600 mg/1 tablet, coated, listed with the FDA by Proficient Rx LP. It has 2 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?
Proficient Rx LP, NDC labeler code 82804. 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 800 mg/1TabletOralSt. Mary's Medical Park Pharmacy60760-94360760-0943-3060760-0943-90
gabapentinGabapentin 300 mg/1CapsuleOralREMEDYREPACK INC.70518-476370518-4763-00
GabapentinGabapentin 100 mg/1CapsuleOralCardinal Health 107, LLC55154-058155154-0581-00
GabapentinGabapentin 100 mg/1CapsuleOralAdvanced Rx of Tennessee, LLC80425-059580425-0595-0180425-0595-0280425-0595-03+1 more
GabapentinGabapentin 300 mg/1CapsuleOralREMEDYREPACK INC.70518-474670518-4746-0070518-4746-0170518-4746-02+1 more
GabapentinGabapentin 100 mg/1CapsuleOralREMEDYREPACK INC.70518-474270518-4742-0070518-4742-02
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

All 562 Gabapentin NDCs

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 600 mg/1Tablet, CoatedOralTAGI Pharma, Inc.51224-021
GabapentinGabapentin 600 mg/1Tablet, CoatedOralA-S Medication Solutions50090-7268
GabapentinGabapentin 600 mg/1Tablet, CoatedOralA-S Medication Solutions50090-7269
GabapentinGabapentin 800 mg/1Tablet, CoatedOralTAGI Pharma, Inc.51224-121
GabapentinGabapentin 600 mg/1Tablet, CoatedOralMullan Pharmaceutical Inc.83301-0001
GabapentinGabapentin 800 mg/1Tablet, CoatedOralMullan Pharmaceutical Inc.83301-0002
GabapentinGabapentin 800 mg/1Tablet, CoatedOralNuCare Pharmaceuticals,Inc.68071-3523
GabapentinGabapentin 800 mg/1Tablet, CoatedOralProficient Rx LP82804-203
GabapentinGabapentin 600 mg/1Tablet, CoatedOralNuCare Pharmaceuticals, Inc.68071-3783
GabapentinGabapentin 600 mg/1Tablet, CoatedOralCoupler LLC67046-1233
GabapentinGabapentin 600 mg/1Tablet, CoatedOralPrecision Dose, Inc.68094-069
GabapentinGabapentin 800 mg/1Tablet, CoatedOralWestminster Pharmaceuticals, LLC69367-347
GabapentinGabapentin 600 mg/1Tablet, CoatedOralWestminster Pharmaceuticals, LLC69367-346
GabapentinGabapentin 600 mg/1Tablet, CoatedOralAvPAK50268-325
GabapentinGabapentin 800 mg/1Tablet, CoatedOralPrecision Dose, Inc.68094-489
GabapentinGabapentin 800 mg/1Tablet, CoatedOralA-S Medication Solutions50090-7400
GabapentinGabapentin 600 mg/1Tablet, CoatedOralPrecision Dose, Inc.68094-589
GabapentinGabapentin 600 mg/1Tablet, CoatedOralBryant Ranch Prepack71335-1287
GabapentinGabapentin 600 mg/1Tablet, CoatedOralAdvanced Rx of Tennessee, LLC80425-0201
GabapentinGabapentin 800 mg/1Tablet, CoatedOralAdvanced Rx of Tennessee, LLC80425-0204

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