NDC codes

FDA NDC Directory
Product NDC (as listed)68084-536Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68084-0536Add 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
68084-536-016808405360168084053601100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-536-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-536-11)Marketed from Apr 24, 2014

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 — 75 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
American Health PackagingNDC labeler code 68084
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 076274
Marketing start
Marketing end
Other FDA classes
Cytochrome P450 2C8 Inhibitors (Mechanism)Decreased Platelet Aggregation (Physiologic effect)P2Y12 Receptor Antagonists (Mechanism)
Identifiers
Product ID 68084-536_5c4015f5-e2ee-77ae-e063-6294a90aa0eaSPL ID 5c4015f5-e2ee-77ae-e063-6294a90aa0ea
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

N468084053601 followed by a unit qualifier and the quantity

Package 68084-0536-01. 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 68084-536

What is NDC 68084-536?
68084-536 is the product NDC for Clopidogrel (clopidogrel bisulfate), Clopidogrel bisulfate 75 mg/1 tablet, film coated, listed with the FDA by American Health Packaging. It has 1 package NDC, 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?
American Health Packaging, NDC labeler code 68084. 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 076274

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

FDA NDC Directory listings under ANDA 076274
ProductStrengthForm · routeLabelerProduct NDC
Clopidogrelclopidogrel bisulfateClopidogrel bisulfate 300 mg/1Tablet, Film coatedOralMajor Pharmaceuticals0904-6467
Clopidogrelclopidogrel bisulfateClopidogrel bisulfate 75 mg/1Tablet, Film coatedOralCardinal Health 107, LLC55154-2149
Clopidogrelclopidogrel bisulfateClopidogrel bisulfate 75 mg/1Tablet, Film coatedOralApotex Corp.60505-0253
Clopidogrelclopidogrel bisulfateClopidogrel bisulfate 300 mg/1Tablet, Film coatedOralApotex Corp.60505-3532
Clopidogrelclopidogrel bisulfateClopidogrel bisulfate 300 mg/1Tablet, Film coatedOralAmerican Health Packaging68084-752
Clopidogrelclopidogrel bisulfateClopidogrel bisulfate 75 mg/1Tablet, Film coatedOralAphena Pharma Solutions - Tennessee, LLC71610-527

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