93 7201
Pill imprint 93 7201 has been identified as Pravastatin sodium 20 mg.
Pravastatin is used in the treatment of high cholesterol; high cholesterol, familial heterozygous; hyperlipoproteinemia; ischemic stroke, prophylaxis; hyperlipoproteinemia type iia, elevated ldl (and more), and belongs to the drug class statins. Not for use in pregnancy.
Pravastatin 20 mg is not subject to the Controlled Substances Act.
See also related documents.
Pravastatin sodium Images
- Imprint:
-
93
7201 - Strength:
- 20 mg
- Color:
- Yellow
- Size:
- 8.00 mm
- Shape:
- Round
- Availability:
- Prescription only
- Inactive Ingredients:
- calcium phosphate dibasic anhydrous
crospovidone
lactose
microcrystalline cellulose
povidone
croscarmellose sodium
ferric oxide yellow
sodium stearyl fumarate
- Drug Class:
- Statins
- Pregnancy Category:
- X - Not for use in pregnancy
- CSA Schedule:
- N - Not a controlled drug
- Manufacturer:
- Teva Pharmaceuticals USA
- National Drug Code (NDC):
- 00093-7201
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More Pravastatin Sodium resources
- Pravastatin (Wolters Kluwer)
- pravastatin (Cerner Multum)
- pravastatin (Micromedex) - Includes Dosage Information
- Pravastatin Sodium (AHFS DI)
- Pravastatin (FDA)
- Pravastatin Sodium (Wolters Kluwer)
Pravastatin Sodium is associated with the treatment of:
- High Cholesterol
- High Cholesterol, Familial Heterozygous
- Hyperlipoproteinemia
- Hyperlipoproteinemia Type IIa, Elevated LDL
- Hyperlipoproteinemia Type IIb, Elevated LDL VLDL
- Hyperlipoproteinemia Type III, Elevated beta-VLDL IDL
- Hyperlipoproteinemia Type IV, Elevated VLDL
- Ischemic Stroke, Prophylaxis
- Myocardial Infarction, Prophylaxis
- Revascularization Procedures, Prophylaxis
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