51655-557 : Levothyroxine Sodium .112 mg Oral Tablet
NDC: | 51655-557 |
Labeler: | Northwind Pharmaceuticals |
Product Type: | Human Prescription Drug |
Drug Name: | Levothyroxine Sodium |
Dosage Form: | Oral Tablet |
Application #: | NDA021210 |
Rev. Date: |
NDC Package Codes:
- 51655-557-52: 30 TABLET IN 1 BOTTLE, PLASTIC (51655‑557‑52)
Active Ingredients:
- Levothyroxine Sodium
Dosage Strength:
- .112 mg
Pharmaceutical Classes:
- Thyroxine [CS]
- l-Thyroxine [EPC]
Related Products:
Based on records with the same trade name.- 51655-095 Levothyroxine Sodium .15 mg Oral Tablet by Northwind Pharmaceuticals
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- 51655-453 Levothyroxine Sodium .05 mg Oral Tablet by Northwind Pharmaceuticals
- 51655-483 Levothyroxine Sodium .088 mg Oral Tablet by Northwind Pharmaceuticals
- 51655-485 Levothyroxine Sodium .137 mg Oral Tablet by Northwind Pharmaceuticals
- 51655-513 Levothyroxine Sodium .137 mg Oral Tablet by Northwind Pharmaceuticals
- 51655-604 Levothyroxine Sodium 112 ug/1 Oral Tablet by Northwind Pharmaceuticals
- 51655-687 Levothyroxine Sodium .075 mg Oral Tablet by Northwind Pharmaceuticals
- 51655-694 Levothyroxine Sodium .15 mg Oral Tablet by Northwind Pharmaceuticals
- 51655-696 Levothyroxine Sodium .125 mg Oral Tablet by Northwind Pharmaceuticals
- 51655-705 Levothyroxine Sodium .088 mg Oral Tablet by Northwind Pharmaceuticals
- 51655-714 Levothyroxine Sodium 175 ug/1 Oral Tablet by Northwind Pharmaceuticals
- 51655-739 Levothyroxine Sodium 50 ug/1 Oral Tablet by Northwind Pharmaceuticals
- 51655-742 Levothyroxine Sodium 100 ug/1 Oral Tablet by Northwind Pharmaceuticals
- 51655-783 Levothyroxine Sodium 150 ug/1 Oral Tablet by Northwind Pharmaceuticals
- 51655-923 Levothyroxine Sodium .1 mg Oral Tablet by Northwind Pharmaceuticals
- 51655-924 Levothyroxine Sodium .05 mg Oral Tablet by Northwind Pharmaceuticals
- 51655-985 Levothyroxine Sodium .025 mg Oral Tablet by Northwind Pharmaceuticals
- 51655-989 Levothyroxine Sodium .075 mg Oral Tablet by Northwind Pharmaceuticals
- More related products ...
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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.