NDC codes

FDA NDC Directory
Product NDC (as listed)68180-222Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68180-0222Add the package segment from the table below.

Product information

Brand name (proprietary)
Niacin
Generic name (nonproprietary)
niacin
Active ingredients
Niacin — 750 mg/1
Dosage form
Tablet, Extended release
Route
Oral
Labeler
Lupin Pharmaceuticals, Inc.NDC labeler code 68180
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 090892
Marketing start
Listing expires
Other FDA classes
Nicotinic Acids (Chemical structure)
Identifiers
Product ID 68180-222_309a40e8-333f-478a-8a94-beff7f3ca5b2SPL ID 309a40e8-333f-478a-8a94-beff7f3ca5b2SPL set ID 92b3ec1d-0dc7-4bde-9817-57b1bdf7f0b9RxCUI 1098134, 1098141, 1098143UNII 2679MF687A
Pharmacologic class
Nicotinic Acid

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.

Product label

Current FDA label (SPL), effective .

Indications (excerpt from the label)

Niacin extended-release tablet USP contains extended-release niacin (nicotinic acid), and is indicated: • To reduce elevated TC, LDL-C, Apo B and TG, and to increase HDL-C in patients with primary hyperlipidemia and mixed dyslipidemia. ( 1 ) • To reduce the risk of recurrent nonfatal myocardial infarction in patients with a history of myocardial infarction and hyperlipidemia. ( 1 ) • In combination with a bile acid binding resin : Slows progression or promotes regression of atherosclerotic disease in patients with a history of coronary artery disease (CAD) and hyperlipidemia. ( 1 ) As an adjunct to diet to reduce elevated TC and LDL-C in adult patients with primary hyperlipidemia. ( 1 ) • To…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 68180-222

What is NDC 68180-222?
68180-222 is the product NDC for Niacin, Niacin 750 mg/1 tablet, extended release, listed with the FDA by Lupin Pharmaceuticals, Inc..
What drug is associated with this NDC?
Niacin.
What is the active ingredient?
Niacin.
Who is the labeler?
Lupin Pharmaceuticals, Inc., NDC labeler code 68180. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Niacin?
22 other product NDCs are listed under this name. See all Niacin 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 Niacin NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
NiacinNiacin 500 mg/1Tablet, Extended releaseOralQUAGEN PHARMACEUTICALS LLC70752-29570752-0295-09
NiacinNiacin 1000 mg/1Tablet, Extended releaseOralQUAGEN PHARMACEUTICALS LLC70752-29670752-0296-09
NiacinNiacin 500 mg/1TabletOralMacleods Pharmaceuticals Limited33342-18733342-0187-1033342-0187-11
NiacinNiacin 1000 mg/1TabletOralMacleods Pharmaceuticals Limited33342-18933342-0189-1033342-0189-11
NiacinNiacin 750 mg/1Tablet, Extended releaseOralAurobindo Pharma Limited59651-01959651-0019-0559651-0019-1859651-0019-90
NiacinNiacin 1000 mg/1Tablet, Extended releaseOralAurobindo Pharma Limited59651-02059651-0020-0559651-0020-1859651-0020-90
NiacinNiacin 500 mg/1Tablet, Extended releaseOralAurobindo Pharma Limited59651-01859651-0018-0559651-0018-1859651-0018-90
NiacinNiacin 500 mg/1Tablet, Extended releaseOralAvPAK50268-58450268-0584-13
NiacinNiacin 1000 mg/1Tablet, Extended releaseOralGolden State Medical Supply, Inc.51407-26851407-0268-90
NiacinNiacin 500 mg/1Tablet, Extended releaseOralGolden State Medical Supply, Inc.51407-26751407-0267-90

All 23 Niacin NDCs

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