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2. Atenolol - Wikipedia

   en.wikipedia.org/wiki/Atenolol

   Atenolol is available in the form of 25, 50, and 100 mg oral tablets. [21] [4] It is also available in the form of oral tablets containing a combination of 50 or 100 mg atenolol and 50 mg chlortalidone. [21] Atenolol was previously available in a 0.5 mg/mL solution for injection as well, but this formulation was discontinued. [21]

3. Atenolol/chlorthalidone - Wikipedia

   en.wikipedia.org/wiki/Atenolol/chlorthalidone

   Atenolol/chlorthalidone, also known as co-tenidone, is a combination medication used to treat high blood pressure. [2] [3] It is made up of atenolol, a beta-blocker and chlortalidone, a diuretic. [4] It is not recommended as an initial treatment but may be used in those who are taking atenolol and chlortalidone individually. [5] It is taken by ...

4. Bisoprolol - Wikipedia

   en.wikipedia.org/wiki/Bisoprolol

   Zebeta 5-mg oral tablet. Bisoprolol is used for prevention of cardiovascular events following a heart attack in patients with risk factors for disease progression, [16] in the management of congestive heart failure with reduced ejection fraction, [17] and as a second-line agent for hypertension.

5. FDA approves first new type of pain medication in 25 years - AOL

   www.aol.com/news/fda-approves-first-type-pain...

   FDA approves first new type of pain medication in 25 years. Brenda Goodman, CNN. ... Vertex said that it has set a wholesale cost of $15.50 per 50-mg pill but that patient assistance programs ...

6. Metoprolol - Wikipedia

   en.wikipedia.org/wiki/Metoprolol

   The specific agent in on-market formulations of metoprolol is either metoprolol tartrate or metoprolol succinate, where tartrate is an immediate-release formulation and the succinate is an extended-release formulation (with 100 mg metoprolol tartrate corresponding to 95 mg metoprolol succinate). [41]

7. Nadolol - Wikipedia

   en.wikipedia.org/wiki/Nadolol

   Four of the stereoisomers of nadolol. Nadolol is a non-selective beta blocker; that is, it non-selectively blocks both beta-1 and beta-2 receptors.It has a preference for beta-1 receptors, which are predominantly located in the heart, thereby inhibiting the effects of catecholamines and causing a decrease in heart rate and blood pressure.