NDC codes

FDA NDC Directory
Product NDC (as listed)68180-288Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68180-0288Add the package segment from the table below.

Product information

Brand name (proprietary)
Abacavir and Lamivudine
Generic name (nonproprietary)
abacavir and lamivudine
Active ingredients
Abacavir sulfate — 600 mg/1Lamivudine — 300 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 204990
Marketing start
Listing expires
Other FDA classes
Cytochrome P450 1A1 Inhibitors (Mechanism)Nucleoside Reverse Transcriptase Inhibitors (Mechanism)Nucleoside Reverse Transcriptase Inhibitors (Mechanism)
Identifiers
Product ID 68180-288_61b0304c-2258-40ed-9fc8-bc363b0906f6SPL ID 61b0304c-2258-40ed-9fc8-bc363b0906f6SPL set ID 1d8e7bb9-8624-4739-9719-fe25109d6365RxCUI 602393UNII J220T4J9Q2, 2T8Q726O95UPC 0368180288060
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)

Abacavir and lamivudine tablet, a combination of abacavir and lamivudine, both nucleoside analogue HIV-1 reverse transcriptase inhibitors, is indicated in combination with other antiretroviral agents for the treatment of HIV-1 infection. ( 1 ) Abacavir and lamivudine tablets, in combination with other antiretroviral agents, are indicated for the treatment of human immunodeficiency virus type 1 (HIV-1) infection.

Excerpt only. Read the full label for complete information.

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