0173-0635 : Leukeran 2 mg Oral Tablet
| NDC: | 0173-0635 |
| Labeler: | Glaxosmithkline LLC |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Leukeran |
| Dosage Form: | Oral Tablet, Film Coated |
| Application #: | NDA010669 |
| Rev. Date: |
Appearance:
| Markings: | GX;EG3;L |
| Shapes: |
Round |
| Colors: |
 Brown |
| Size (mm): | 7 |
| 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:
- 0173-0635-35: 50 TABLET, FILM COATED IN 1 BOTTLE (0173‑0635‑35)
Active Ingredients:
- Chlorambucil
Dosage Strength:
- 2 mg
Inactive Ingredients:
- Silicon Dioxide
- Hypromelloses
- Anhydrous Lactose
- Polyethylene Glycol
- Cellulose, Microcrystalline
- Ferric Oxide Red
- Stearic Acid
- Titanium Dioxide
- Ferric Oxide Yellow
Pharmaceutical Classes:
- Alkylating Activity [MoA]
- Alkylating Drug [EPC]
Related Products:
Based on records with the same trade name.- 69784-610 Leukeran 2 mg Oral Tablet, Film Coated by Woodward Pharma Services LLC
- 76388-635 Leukeran 2 mg Oral Tablet by Aspen Global Inc.
- 80725-610 Leukeran 2 mg Oral Tablet, Film Coated by Waylis Therapeutics LLC
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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.