0056-0510 : Sustiva 600 mg Oral Tablet
NDC: | 0056-0510 |
Labeler: | Bristol-myers Squibb Pharma Company |
Product Type: | Human Prescription Drug |
Drug Name: | Sustiva |
Dosage Form: | Oral Tablet, Film Coated |
Application #: | NDA021360 |
Rev. Date: |
Appearance:
Markings: | SUSTIVA;SUSTIVA |
Shapes: |
Oval |
Colors: |
Yellow |
Size (mm): | 19 |
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. |
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:
- 0056-0510-30: 30 TABLET, FILM COATED IN 1 BOTTLE (0056‑0510‑30)
Active Ingredients:
- Efavirenz
Dosage Strength:
- 600 mg
Inactive Ingredients:
- Croscarmellose Sodium
- Hydroxypropyl Cellulose
- Lactose Monohydrate
- Magnesium Stearate
- Cellulose, Microcrystalline
- Sodium Lauryl Sulfate
- Carnauba Wax
Pharmaceutical Classes:
- Human Immunodeficiency Virus 1 Non-Nucleoside Analog Reverse Transcriptase Inhibitor [EPC]
- Non-Nucleoside Analog [Chemical/Ingredient]
- Non-Nucleoside Reverse Transcriptase Inhibitors [MoA]
- Cytochrome P450 3A Inducers [MoA]
- Cytochrome P450 2B6 Inducers [MoA]
- Cytochrome P450 2C9 Inhibitors [MoA]
- Cytochrome P450 2C19 Inhibitors [MoA]
- Cytochrome P450 3A4 Inhibitors [MoA]
Related Products:
Based on records with the same trade name.- 0056-0470 Sustiva 50 mg Oral Capsule by Bristol-myers Squibb Pharma Company
- 0056-0474 Sustiva 200 mg Oral Capsule by Bristol-myers Squibb Pharma Company
- 24236-282 Sustiva 600 mg Oral Tablet, Film Coated by Remedyrepack Inc.
- 43798-015 Sustiva 50 mg Oral Capsule by Aesica Queenborough Limited
- 43798-016 Sustiva 200 mg Oral Capsule by Aesica Queenborough Limited
- 54569-5374 Sustiva 600 mg Oral Tablet, Film Coated by A-s Medication Solutions
- 54868-4668 Sustiva 600 mg Oral Tablet by Physicians Total Care, Inc.
- 70518-0482 Sustiva 600 mg Oral Tablet, Film Coated by Remedyrepack Inc.
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.