70934-520 : Levothyroxine Sodium .175 mg Oral Tablet
| NDC: | 70934-520 |
| Labeler: | Denton Pharma, Inc. Dba Northwind Pharmaceuticals |
| Product Type: | Human Prescription Drug |
| Drug Name: | Levothyroxine Sodium |
| Dosage Form: | Oral Tablet |
| Application #: | ANDA209713 |
| Rev. Date: |
NDC Package Codes:
- 69097-314-42: 1 VIAL, SINGLE‑USE IN 1 CARTON (69097‑314‑42) > 25 ML IN 1 VIAL, SINGLE‑USE
Active Ingredients:
- Gemcitabine Hydrochloride
Dosage Strength:
- 1 g/25mL
Pharmaceutical Classes:
- Nucleic Acid Synthesis Inhibitors [MoA]
- Nucleoside Metabolic Inhibitor [EPC]
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- 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.