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metoprolol tartrate 25 MG Oral Tablet

INDICATIONS AND USAGE Hypertension Metoprolol tartrate tablets, USP are indicated for the treatment of Hypertension. They may be used alone or in combination with other antihypertensive agents. Angina Pectoris Metoprolol tartrate tablets, USP are indicated in the long-term treatment of Angina Pectoris. Myocardial Infarction Metoprolol tartrate tablets, USP are indicated in the treatment of hemodynamically stable patients with definite or suspected acute Myocardial Infarction to reduce cardiovascular mortality when used alone or in conjunction with intravenous metoprolol. Oral metoprolol tartrate tablets, USP therapy can be initiated after intravenous metoprolol therapy or, alternatively, oral treatment can begin within 3 to 10 days of the acute event (see DOSAGE AND ADMINISTRATION , CONTRAINDICATIONS , and WARNINGS ).

Aphena Pharma Solutions - Tennessee, LLC


4 months ago ROUND WHITE C 73 metoprolol tartrate 25 MG Oral Tablet

ROUND WHITE C 73

4 months ago ROUND WHITE C 73 metoprolol tartrate 25 MG Oral Tablet

C 73 ROUND WHITE

HOW SUPPLIED Repackaged by Aphena Pharma Solutions - TN. See Repackaging Information for available configurations. Metoprolol Tartrate Tablets, USP are available as follows: Tablets 25 mg are white round shaped, film coated tablets debossed with ‘C over 73’ on one side and deep break line on other side. Bottles of 100 NDC 52343-059-01 (Child Resistant Closure) Bottles of 1000 NDC 52343-059-99 (Non Child Resistant Closure) Tablets 50 mg are pink round shaped, film coated tablets debossed with ‘C over 74’ on one side and deep break line on other side. Bottles of 100 NDC 52343-060-01 (Child Resistant Closure) Bottles of 1000 NDC 52343-060-99 (Non Child Resistant Closure) Tablets 100 mg are light blue round shaped, film coated tablets debossed with ‘C over 75’ on one side and deep break line on other side. Bottles of 100 NDC 52343-061-01 (Child Resistant Closure) Bottles of 1000 NDC 52343-061-99 (Non Child Resistant Closure) Store at 20° to 25 °C (68° to 77 °F); excursions permitted to 15 ° to 30 °C (59 ° to 86 °F) [see USP Controlled Room Temperature ]. Protect from moisture and heat. Dispense in a tight, light-resistant container as defined in the USP using a child-resistant closure. To report SUSPECTED ADVERSE REACTIONS, contact Gen-Source Rx at 1-877-443-6768 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch Manufactured for: Cedardale Distributors, LLC D/B/A Gen-Source RX 620 Gotham Parkway Carlstadt, NJ 07072 USA Manufactured by: Aurolife Pharma LLC Dayton, NJ 08810 Issued: 03/2014


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