NDC codes

FDA NDC Directory
Product NDC (as listed)82804-986Labeler and product segments. Claims need a package NDC.
Product NDC at billing width82804-0986Add 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
82804-986-008280409860082804098600100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82804-986-00)Marketed from May 21, 2024
82804-986-30828040986308280409863030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82804-986-30)Marketed from May 21, 2024
82804-986-558280409865582804098655500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82804-986-55)Marketed from May 21, 2024
82804-986-60828040986608280409866060 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82804-986-60)Marketed from May 21, 2024
82804-986-648280409866482804098664240 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82804-986-64)Marketed from May 21, 2024
82804-986-728280409867282804098672120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82804-986-72)Marketed from May 21, 2024
82804-986-788280409867882804098678180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82804-986-78)Marketed from May 21, 2024
82804-986-90828040986908280409869090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82804-986-90)Marketed from May 21, 2024

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)
Clopidogrel
Generic name (nonproprietary)
clopidogrel bisulfate
Active ingredients
Clopidogrel bisulfate — 300 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
Proficient Rx LPNDC labeler code 82804
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 204165
Marketing start
Listing expires
Other FDA classes
Cytochrome P450 2C8 Inhibitors (Mechanism)Decreased Platelet Aggregation (Physiologic effect)P2Y12 Receptor Antagonists (Mechanism)
Identifiers
Product ID 82804-986_330702d9-842c-416d-9b11-b4a9b707e9b2SPL ID 330702d9-842c-416d-9b11-b4a9b707e9b2SPL set ID 330702d9-842c-416d-9b11-b4a9b707e9b2RxCUI 749196UNII 08I79HTP27UPC 0382804986309
Pharmacologic class
P2Y12 Platelet Inhibitor

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

N482804098600 followed by a unit qualifier and the quantity

Package 82804-0986-00. 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

Current FDA label (SPL), effective . This label includes a boxed warning.

Indications (excerpt from the label)

Clopidogrel is a P2Y 12 platelet inhibitor indicated for: • Acute coronary syndrome 1. For patients with non–ST-segment elevation ACS (unstable angina [UA]/non–ST-elevation myocardial infarction [NSTEMI]), clopidogrel has been shown to reduce the rate of myocardial infarction (MI) and stroke. ( 1.1 ) 2. For patients with ST-elevation myocardial infarction (STEMI), clopidogrel has been shown to reduce the rate of MI and stroke. ( 1.1 ) • Recent MI, recent stroke, or established peripheral arterial disease. Clopidogrel has been shown to reduce the rate of MI and stroke. ( 1.2 ) 1.1 Acute Coronary Syndrome (ACS) • Clopidogrel is indicated to reduce the rate of myocardial infarction (MI) and str…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 82804-986

What is NDC 82804-986?
82804-986 is the product NDC for Clopidogrel (clopidogrel bisulfate), Clopidogrel bisulfate 300 mg/1 tablet, film coated, listed with the FDA by Proficient Rx LP. It has 8 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Clopidogrel (Clopidogrel Bisulfate).
What is the active ingredient?
Clopidogrel bisulfate.
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 Clopidogrel?
41 other product NDCs are listed under this name. See all Clopidogrel 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 Clopidogrel NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Clopidogrelclopidogrel bisulfateClopidogrel bisulfate 75 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals Inc.68788-417368788-4173-0368788-4173-0668788-4173-09
Clopidogrelclopidogrel bisulfateClopidogrel bisulfate 75 mg/1Tablet, Film coatedOralCardinal Health 107, LLC55154-214955154-2149-00
Clopidogrelclopidogrel bisulfateClopidogrel bisulfate 75 mg/1TabletOralREMEDYREPACK INC.70518-437370518-4373-00
Clopidogrelclopidogrel bisulfateClopidogrel bisulfate 75 mg/1Tablet, Film coatedOralNovadoz Pharmaceuticals LLC72205-19972205-0199-0172205-0199-0572205-0199-06+2 more
Clopidogrelclopidogrel bisulfateClopidogrel bisulfate 75 mg/1TabletOralA-S Medication Solutions50090-746650090-7466-0050090-7466-01
Clopidogrelclopidogrel bisulfateClopidogrel bisulfate 75 mg/1TabletOralA-S Medication Solutions50090-746750090-7467-00
Clopidogrelclopidogrel bisulfateClopidogrel bisulfate 75 mg/1TabletOralAscend Laboratories, LLC67877-27667877-0276-0567877-0276-3067877-0276-90
ClopidogrelClopidogrel 75 mg/1TabletOralCamber Pharmaceuticals, Inc.31722-75831722-0758-0531722-0758-3031722-0758-90
ClopidogrelClopidogrel 300 mg/1TabletOralCamber Pharmaceuticals, Inc.31722-75931722-0759-0531722-0759-30
Clopidogrelclopidogrel bisulfateClopidogrel bisulfate 75 mg/1Tablet, Film coatedOralWestminster Pharmaceuticals, LLC69367-20069367-0200-05

All 42 Clopidogrel NDCs

Other NDCs under ANDA 204165

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

FDA NDC Directory listings under ANDA 204165
ProductStrengthForm · routeLabelerProduct NDC
ClopidogrelClopidogrel bisulfate 75 mg/1TabletOralVensun Pharmaceuticals, Inc.42543-713
ClopidogrelClopidogrel bisulfate 300 mg/1TabletOralVensun Pharmaceuticals, Inc.42543-714
Clopidogrelclopidogrel bisulfateClopidogrel bisulfate 300 mg/1Tablet, Film coatedOralAvPAK50268-184
Clopidogrelclopidogrel bisulfateClopidogrel bisulfate 300 mg/1Tablet, Film coatedOralWestminster Pharmaceuticals, LLC69367-194
Clopidogrelclopidogrel bisulfateClopidogrel bisulfate 75 mg/1Tablet, Film coatedOralWestminster Pharmaceuticals, LLC69367-200
Clopidogrel bisulfateClopidogrel bisulfate 75 mg/1Tablet, Film coatedOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8625
Clopidogrel bisulfateClopidogrel bisulfate 300 mg/1Tablet, Film coatedOralScieGen Pharmaceuticals Inc50228-121
Clopidogrel bisulfateClopidogrel bisulfate 75 mg/1Tablet, Film coatedOralScieGen Pharmaceuticals Inc50228-124
Clopidogrel bisulfateClopidogrel bisulfate 75 mg/1Tablet, Film coatedOralProficient Rx LP63187-639
Clopidogrel bisulfateClopidogrel bisulfate 75 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals,Inc.68071-5277
Clopidogrel bisulfateClopidogrel bisulfate 75 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals, Inc.68788-7700
Clopidogrel bisulfateClopidogrel bisulfate 75 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-4110
Clopidogrel bisulfateClopidogrel bisulfate 75 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-1646
Clopidogrel bisulfateClopidogrel bisulfate 75 mg/1Tablet, Film coatedOralBryant Ranch Prepack72162-2212
Clopidogrel bisulfateClopidogrel bisulfate 300 mg/1Tablet, Film coatedOralRADHA PHARMACEUTICALS, INC.77771-121
Clopidogrel bisulfateClopidogrel bisulfate 75 mg/1Tablet, Film coatedOralRADHA PHARMACEUTICALS, INC.77771-124

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