53808-0843 : Lamivudine 150 mg Oral Tablet, Film Coated
NDC: | 53808-0843 |
Labeler: | State of Florida Doh Central Pharmacy |
Product Type: | Human Prescription Drug |
Drug Name: | Lamivudine |
Dosage Form: | Oral Tablet, Film Coated |
Application #: | ANDA091606 |
Rev. Date: |
Appearance:
Markings: | APO;LMV;150 |
Shapes: |
Diamond (4 sides) |
Colors: |
White |
Size (mm): | 14 |
Segments: * | 2 |
* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 2 indicates a scored pill which can be broken into 2 equal pieces. |
The above image is provided by the U.S. National Library of Medicine (NLM) and is not part of the official label.
NDC Package Codes:
- 53808-0843-1: 30 TABLET, FILM COATED IN 1 BLISTER PACK (53808‑0843‑1)
Active Ingredients:
- Lamivudine
Dosage Strength:
- 150 mg
Inactive Ingredients:
- Anhydrous Lactose
- Crospovidone
- Colloidal Silicon Dioxide
- Hypromelloses
- Hydroxypropyl Cellulose
- Magnesium Stearate
- Polyethylene Glycols
- Titanium Dioxide
Pharmaceutical Classes:
- Hepatitis B Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC]
- Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC]
- Nucleoside Analog [EXT]
- Nucleoside Reverse Transcriptase Inhibitors [MoA]
Related Products:
Based on records with the same trade name.- 53808-0844 Lamivudine 300 mg Oral Tablet, Film Coated by State of Florida Doh Central Pharmacy
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- 50742-623 Lamivudine 150 mg Oral Tablet by Ingenus Pharmaceuticals, LLC
- 50742-624 Lamivudine 300 mg Oral Tablet by Ingenus Pharmaceuticals, LLC
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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.