Lamivudine and Zidovudine
- Product NDC
- 65862-036
- 11-digit product format
- 658620036
- Labeler code
- 65862
- Product ID
- 65862-036_c4e0edda-dad5-4bed-b108-b6aae30e3be3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lamivudine and Zidovudine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Aurobindo Pharma Limited
- Application
- ANDA077558
- Marketing category
- ANDA
- Marketing start
- 2017-05-05
- Substance
- LAMIVUDINE; ZIDOVUDINE
- Active strength
- 150; 300 mg/1; mg/1
- Pharmacologic classes
- 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
- Lamivudine and Zidovudine
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| LAMIVUDINE | 150 mg/1 |
| ZIDOVUDINE | 300 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 2T8Q726O95, 4B9XT59T7S |
| Rxcui | 200082 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 65862-036-10 | Lamivudine and Zidovudine | 10 in 1 BLISTER PACK | TABLET, FILM COATED | 10 | | 6 |
| 65862-036-10 | Lamivudine and Zidovudine | 6 in 1 CARTON | TABLET, FILM COATED | 6 | | 6 |
| 65862-036-60 | Lamivudine and Zidovudine | 60 in 1 BOTTLE | TABLET, FILM COATED | 60 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 65862-036 | LAMIVUDINE AND ZIDOVUDINE TABLET, FILM COATED [AUROBINDO PHARMA LIMITED] | 6 | Current NDC, Legacy NDC, 3 package rows | 20240529_d40292ff-046c-4a04-b801-10768667951a.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 65862-036-10 | 65862003610 | 6 BLISTER PACK in 1 CARTON (65862-036-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK | 6 blister pack | 2017-05-05 | 0000-00-00 | No | No | Current |
| 65862-036-60 | 65862003660 | 60 TABLET, FILM COATED in 1 BOTTLE (65862-036-60) | | 2017-05-05 | 0000-00-00 | No | No | Current |