Abacavir and Lamivudine
- Product NDC
- 68180-288
- 11-digit product format
- 681800288
- Labeler code
- 68180
- Product ID
- 68180-288_61b0304c-2258-40ed-9fc8-bc363b0906f6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Abacavir and Lamivudine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Lupin Pharmaceuticals, Inc.
- Application
- ANDA204990
- Marketing category
- ANDA
- Marketing start
- 2017-03-28
- Substance
- ABACAVIR SULFATE; LAMIVUDINE
- Active strength
- 600; 300 mg/1; mg/1
- Pharmacologic classes
- Cytochrome P450 1A1 Inhibitors [MoA], Hepatitis B Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC], Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC], Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC], Nucleoside Reverse Transcriptase Inhibitors [MoA], Nucleoside Reverse Transcriptase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Abacavir and Lamivudine
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ABACAVIR SULFATE | 600 mg/1 |
| LAMIVUDINE | 300 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | J220T4J9Q2, 2T8Q726O95 |
| Rxcui | 602393 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68180-288-06 | Abacavir and Lamivudine | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 14 |
| 68180-288-09 | Abacavir and Lamivudine | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | | 14 |
| 68180-288-33 | Abacavir and Lamivudine | 750 in 1 POUCH | TABLET, FILM COATED | 750 | | 14 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68180-288 | ABACAVIR AND LAMIVUDINE TABLET, FILM COATED [LUPIN PHARMACEUTICALS, INC.] | 14 | Current NDC, Legacy NDC, 3 package rows | 20231031_1d8e7bb9-8624-4739-9719-fe25109d6365.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68180-288-06 | 68180028806 | 30 TABLET, FILM COATED in 1 BOTTLE (68180-288-06) | 2017-03-28 | 0000-00-00 | No | No | Current |
| 68180-288-09 | 68180028809 | 90 TABLET, FILM COATED in 1 BOTTLE (68180-288-09) | 2017-03-28 | 0000-00-00 | No | No | Current |
| 68180-288-33 | 68180028833 | 750 TABLET, FILM COATED in 1 POUCH (68180-288-33) | 2017-03-28 | 0000-00-00 | No | No | Current |