Prescription drug · ANDA
Abacavir and Lamivudine NDC 68180-288
Abacavir sulfate 600 mg/1; Lamivudine 300 mg/1 · Tablet, Film coated · Oral · Lupin Pharmaceuticals, Inc.
NDC codes
FDA NDC DirectoryProduct 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
- Labeler
- Lupin Pharmaceuticals, Inc.NDC labeler code 68180
- 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.
About NDC 68180-288
- What is NDC 68180-288?
- 68180-288 is the product NDC for Abacavir and Lamivudine, Abacavir sulfate 600 mg/1; Lamivudine 300 mg/1 tablet, film coated, listed with the FDA by Lupin Pharmaceuticals, Inc..
- What drug is associated with this NDC?
- Abacavir and Lamivudine.
- What is the active ingredient?
- Abacavir sulfate, 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 Abacavir and Lamivudine?
- 5 other product NDCs are listed under this name. See all Abacavir and Lamivudine NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Abacavir and Lamivudine products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| ABACAVIR and LAMIVUDINE | Abacavir sulfate 600 mg/1; Lamivudine 300 mg/1 | Tablet, Film coatedOral | Camber Pharmaceuticals, Inc. | 31722-838 | 31722-0838-30 |
| Abacavir and Lamivudine | Abacavir sulfate 600 mg/1; Lamivudine 300 mg/1 | Tablet, Film coatedOral | Macleods Pharmaceuticals Limited | 33342-440 | 33342-0440-0733342-0440-1433342-0440-98 |
| Abacavir and Lamivudine | Abacavir sulfate 600 mg/1; Lamivudine 300 mg/1 | Tablet, Film coatedOral | Laurus Labs Limited | 42385-962 | 42385-0962-1842385-0962-3042385-0962-90 |
| Abacavir and Lamivudine | Abacavir sulfate 600 mg/1; Lamivudine 300 mg/1 | Tablet, Film coatedOral | Aurobindo Pharma Limited | 65862-335 | 65862-0335-1065862-0335-30 |
| Abacavir and Lamivudine | Abacavir sulfate 600 mg/1; Lamivudine 300 mg/1 | Tablet, Film coatedOral | Cipla USA Inc. | 69097-362 | 69097-0362-02 |