0179-0152 : Lamivudine 100 mg Oral Tablet, Film Coated
NDC: | 0179-0152 |
Labeler: | Kaiser Foundation Hospitals |
Product Type: | Human Prescription Drug |
Drug Name: | Lamivudine |
Dosage Form: | Oral Tablet, Film Coated |
Application #: | ANDA202941 |
Rev. Date: |
Appearance:
Markings: | APO;LMV100 |
Shapes: |
Oval |
Colors: |
Orange |
Size (mm): | 12 |
Segments: * | 1 |
* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines. |
NDC Package Codes:
- 0179-0152-70: 30 TABLET, FILM COATED IN 1 BOX, UNIT‑DOSE (0179‑0152‑70)
Active Ingredients:
- Lamivudine
Dosage Strength:
- 100 mg
Inactive Ingredients:
- Anhydrous Lactose
- Crospovidone
- Colloidal Silicon Dioxide
- Magnesium Stearate
- Hypromellose 2910 (5 Mpa.s)
- Hydroxypropyl Cellulose
- Polyethylene Glycols
- Titanium Dioxide
- Ferric Oxide Red
- Ferric Oxide Yellow
Pharmaceutical Classes:
- Hepatitis B Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC]
- Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC]
- Nucleoside Analog [Chemical/Ingredient]
- Nucleoside Reverse Transcriptase Inhibitors [MoA]
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- 51293-832 Lamivudine 150 mg Oral Tablet by Eci Pharmaceuticals LLC
- 52125-016 3tc 300 mg Oral Tablet by Remedyrepack Inc.
- 53808-0843 Lamivudine 150 mg Oral Tablet, Film Coated by State of Florida Doh Central Pharmacy
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NDC QR Code
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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.