NDC codes

FDA NDC Directory
Product NDC (as listed)68180-602Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68180-0602Add the package segment from the table below.

Product information

Brand name (proprietary)
Lamivudine
Generic name (nonproprietary)
lamivudine
Active ingredients
Lamivudine — 150 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
Lupin Pharmaceuticals, Inc.NDC labeler code 68180
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 205217
Marketing start
Listing expires
Other FDA classes
Nucleoside Reverse Transcriptase Inhibitors (Mechanism)
Identifiers
Product ID 68180-602_0852eda3-c1d3-426d-b73d-c7f08dfd9584SPL ID 0852eda3-c1d3-426d-b73d-c7f08dfd9584SPL set ID ff3b5265-f533-4332-a861-d8c9c1664ffdRxCUI 199147, 349491UNII 2T8Q726O95UPC 0368180603061, 0368180602071
Pharmacologic class
Hepatitis B Virus Nucleoside Analog Reverse Transcriptase Inhibitor; Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase 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.

Product label

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

Indications (excerpt from the label)

Lamivudine tablets are a nucleoside analogue reverse transcriptase inhibitor indicated in combination with other antiretroviral agents for the treatment of HIV-1 infection. Limitations of Use: The dosage of this product is for HIV-1 and not for HBV. ( 1 ) Lamivudine tablets are a nucleoside analogue indicated in combination with other antiretroviral agents for the treatment of human immunodeficiency virus type 1(HIV-1) infection. Limitations of Use The dosage of this product is for HIV-1 and not for HBV.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 68180-602

What is NDC 68180-602?
68180-602 is the product NDC for Lamivudine, Lamivudine 150 mg/1 tablet, film coated, listed with the FDA by Lupin Pharmaceuticals, Inc..
What drug is associated with this NDC?
Lamivudine.
What is the active ingredient?
Lamivudine.
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 Lamivudine?
24 other product NDCs are listed under this name. See all Lamivudine 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 Lamivudine NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
LamivudineLamivudine 150 mg/1Tablet, Film coatedOralCoupler LLC67046-145967046-1459-03
LamivudineLamivudine 150 mg/1Tablet, Film coatedOralAmerican Health Packaging60687-72060687-0720-21
LamivudineLamivudine 150 mg/1Tablet, Film coatedOralMacleods Pharmaceuticals Limited33342-00133342-0001-09
LamivudineLamivudine 300 mg/1Tablet, Film coatedOralMacleods Pharmaceuticals Limited33342-00233342-0002-07
lamivudineLamivudine 100 mg/1Tablet, Film coatedOralCamber Pharmaceuticals, Inc.31722-00131722-0001-0231722-0001-60
LamivudineLamivudine 150 mg/1Tablet, Film coatedOralStrides Pharma Science Limited64380-71064380-0710-03
LamivudineLamivudine 300 mg/1Tablet, Film coatedOralStrides Pharma Science Limited64380-71164380-0711-04
LamivudineLamivudine 150 mg/1TabletOralIngenus Pharmaceuticals, LLC50742-62350742-0623-60
LamivudineLamivudine 300 mg/1TabletOralIngenus Pharmaceuticals, LLC50742-62450742-0624-60
LamivudineLamivudine 10 mg/mLSolutionOralRising Pharma Holdings, Inc.57237-27457237-0274-24

All 25 Lamivudine NDCs

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