NDC 46708-692 Prazosin Hydrochloride
Capsule Oral
Product Information
Product Characteristics
Color(s) | WHITE (C48325 - OPAQUE WHITE CAP) WHITE (C48325 - OPAQUE WHITE BODY) PINK (C48328 - OPAQUE PINK CAP) |
Shape | CAPSULE (C48336) |
Size(s) | 14 MM 18 MM |
Imprint(s) | A;320 A;321 |
Score | 1 |
Product Packages
NDC Code 46708-692-31
Package Description: 100 CAPSULE in 1 BOTTLE
NDC Code 46708-692-61
Package Description: 250 CAPSULE in 1 BOTTLE
NDC Code 46708-692-91
Package Description: 1000 CAPSULE in 1 BOTTLE
Product Details
What is NDC 46708-692?
The NDC code 46708-692 is assigned by the FDA to the product Prazosin Hydrochloride which is a human prescription drug product labeled by Alembic Pharmaceuticals Limited. The product's dosage form is capsule and is administered via oral form. The product is distributed in 3 packages with assigned NDC codes 46708-692-31 100 capsule in 1 bottle , 46708-692-61 250 capsule in 1 bottle , 46708-692-91 1000 capsule in 1 bottle . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.
What are the uses for Prazosin Hydrochloride?
Prazosin hydrochloride capsules are indicated for the treatment of hypertension, to lower blood pressure. Lowering blood pressure reduces the risk of fatal and nonfatal cardiovascular events, primarily strokes and myocardial infarctions. These benefits have been seen in controlled trials of antihypertensive drugs from a wide variety of pharmacologic classes, including this drug.Control of high blood pressure should be part of comprehensive cardiovascular risk management, including, as appropriate, lipid control, diabetes management, antithrombotic therapy, smoking cessation, exercise, and limited sodium intake. Many patients will require more than one drug to achieve blood pressure goals. For specific advice on goals and management, see published guidelines, such as those of the National High Blood Pressure Education Program’s Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure (JNC).Numerous antihypertensive drugs, from a variety of pharmacologic classes and with different mechanisms of action, have been shown in randomized controlled trials to reduce cardiovascular morbidity and mortality, and it can be concluded that it is blood pressure reduction, and not some other pharmacologic property of the drugs, that is largely responsible for those benefits. The largest and most consistent cardiovascular outcome benefit has been a reduction in the risk of stroke, but reductions in myocardial infarction and cardiovascular mortality also have been seen regularly.Elevated systolic or diastolic pressure causes increased cardiovascular risk, and the absolute risk increase per mmHg is greater at higher blood pressures, so that even modest reductions of severe hypertension can provide substantial benefit. Relative risk reduction from blood pressure reduction is similar across populations with varying absolute risk, so the absolute benefit is greater in patients who are at higher risk independent of their hypertension (for example, patients with diabetes or hyperlipidemia), and such patients would be expected to benefit from more aggressive treatment to a lower blood pressure goal.Some antihypertensive drugs have smaller blood pressure effects (as monotherapy) in black patients, and many antihypertensive drugs have additional approved indications and effects (e.g., on angina, heart failure, or diabetic kidney disease). These considerations may guide selection of therapy.Prazosin hydrochloride capsules can be used alone or in combination with other antihypertensive drugs such as diuretics or beta-adrenergic blocking agents.
What are Prazosin Hydrochloride Active Ingredients?
An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
- PRAZOSIN HYDROCHLORIDE 2 mg/1 - A selective adrenergic alpha-1 antagonist used in the treatment of HEART FAILURE; HYPERTENSION; PHEOCHROMOCYTOMA; RAYNAUD DISEASE; PROSTATIC HYPERTROPHY; and URINARY RETENTION.
Which are Prazosin Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- PRAZOSIN HYDROCHLORIDE (UNII: X0Z7454B90)
- PRAZOSIN (UNII: XM03YJ541D) (Active Moiety)
What is the NDC to RxNorm Crosswalk for Prazosin Hydrochloride?
RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
- RxCUI: 198141 - prazosin HCl 5 MG Oral Capsule
- RxCUI: 198141 - prazosin 5 MG Oral Capsule
- RxCUI: 198141 - prazosin (as prazosin HCl) 5 MG Oral Capsule
- RxCUI: 312593 - prazosin HCl 1 MG Oral Capsule
- RxCUI: 312593 - prazosin 1 MG Oral Capsule
Which are Prazosin Hydrochloride Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- SUCROSE (UNII: C151H8M554)
- STARCH, CORN (UNII: O8232NY3SJ)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- GELATIN, UNSPECIFIED (UNII: 2G86QN327L)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- SHELLAC (UNII: 46N107B71O)
- POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C RED NO. 3 (UNII: PN2ZH5LOQY)
Which are the Pharmacologic Classes for Prazosin Hydrochloride?
A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients of this product.
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Product Label
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