0378-0551 : Tolazamide 500 mg Oral Tablet
| NDC: | 0378-0551 |
| Labeler: | Mylan Pharmaceuticals Inc. |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Tolazamide |
| Dosage Form: | Oral Tablet |
| Application #: | ANDA070259 |
| Rev. Date: |
Appearance:
| Markings: | MYLAN;551 |
| Shapes: |
Round |
| Colors: |
 White |
| Size (mm): | 13 |
| 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. | |
NDC Package Codes:
- 0378-0551-01: 100 TABLET IN 1 BOTTLE, PLASTIC (0378‑0551‑01)
Active Ingredients:
- Tolazamide
Dosage Strength:
- 500 mg
Inactive Ingredients:
- Silicon Dioxide
- Croscarmellose Sodium
- Magnesium Stearate
- Cellulose, Microcrystalline
- Sodium Lauryl Sulfate
Pharmaceutical Classes:
- Sulfonylurea [EPC]
- Sulfonylurea Compounds [CS]
Related Products:
Based on records with the same trade name.- 0378-0217 Tolazamide 250 mg Oral Tablet by Mylan Pharmaceuticals Inc.
- 53489-151 Tolazamide 100 mg Oral Tablet by Mutual Pharmaceutical Company, Inc
- 53489-152 Tolazamide 250 mg Oral Tablet by Mutual Pharmaceutical Company, Inc
- 53489-153 Tolazamide 500 mg Oral Tablet by Mutual Pharmaceutical Company, Inc
- 55289-265 Tolazamide 250 mg Oral Tablet by Pd-rx Pharmaceuticals, Inc.
- 68084-556 Tolazamide 250 mg Oral Tablet by American Health Packaging
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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.