53808-0878 : Zidovudine 300 mg Oral Tablet, Film Coated
NDC: | 53808-0878 |
Labeler: | State of Florida Doh Central Pharmacy |
Product Type: | Human Prescription Drug |
Drug Name: | Zidovudine |
Dosage Form: | Oral Tablet, Film Coated |
Application #: | ANDA078922 |
Rev. Date: |
Appearance:
Markings: | M;106 |
Shapes: |
Round |
Colors: |
White |
Size (mm): | 10 |
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:
- 53808-0878-2: 60 TABLET, FILM COATED IN 1 BLISTER PACK (53808‑0878‑2)
Active Ingredients:
- Zidovudine
Dosage Strength:
- 300 mg
Inactive Ingredients:
- Hypromelloses
- Magnesium Stearate
- Cellulose, Microcrystalline
- Polyethylene Glycols
- Sodium Starch Glycolate Type a Potato
- Titanium Dioxide
Pharmaceutical Classes:
- Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC]
- Nucleoside Analog [EXT]
- Nucleoside Reverse Transcriptase Inhibitors [MoA]
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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.