50090-2207 : Metoprolol Tartrate 25 mg Oral Tablet, Film Coated
NDC: | 50090-2207 |
Labeler: | A-s Medication Solutions |
Product Type: | Human Prescription Drug |
Drug Name: | Metoprolol Tartrate |
Dosage Form: | Oral Tablet, Film Coated |
Application #: | ANDA077739 |
Rev. Date: |
Appearance:
Markings: | C;73 |
Shapes: |
Round |
Colors: |
White |
Size (mm): | 7 |
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. |
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:
- 50090-2207-0: 180 TABLET, FILM COATED IN 1 BOTTLE (50090‑2207‑0)
- 50090-2207-1: 60 TABLET, FILM COATED IN 1 BOTTLE (50090‑2207‑1)
- 50090-2207-2: 90 TABLET, FILM COATED IN 1 BOTTLE (50090‑2207‑2)
- 50090-2207-3: 30 TABLET, FILM COATED IN 1 BOTTLE (50090‑2207‑3)
Active Ingredients:
- Metoprolol Tartrate
Dosage Strength:
- 25 mg
Inactive Ingredients:
- Microcrystalline Cellulose
- Starch, Corn
- Sodium Starch Glycolate Type a Potato
- Silicon Dioxide
- Sodium Lauryl Sulfate
- Talc
- Magnesium Stearate
- Hypromellose 2910 (6 Mpa.s)
- Titanium Dioxide
- Polyethylene Glycol 400
- Polysorbate 80 /
Pharmaceutical Classes:
- Adrenergic beta-Antagonists [MoA]
- beta-Adrenergic Blocker [EPC]
Related Products:
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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.