NDC 67046-208 Prazosin Hydrochloride

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
67046-208
Proprietary Name:
Prazosin Hydrochloride
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Contract Pharmacy Services-pa
Labeler Code:
67046
Start Marketing Date: [9]
09-21-2017
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
GREEN (C48329 - DARK GREEN OPAQUE)
BROWN (C48332 - LIGHT BROWN OPAQUE)
BROWN (C48332 - BROWN OPAQUE)
Shape:
CAPSULE (C48336)
Size(s):
18 MM
Imprint(s):
MYLAN;1101
MYLAN;2302
Score:
1

Product Packages

NDC Code 67046-208-07

Package Description: 7 CAPSULE in 1 BLISTER PACK

NDC Code 67046-208-14

Package Description: 14 CAPSULE in 1 BLISTER PACK

NDC Code 67046-208-15

Package Description: 15 CAPSULE in 1 BLISTER PACK

NDC Code 67046-208-20

Package Description: 20 CAPSULE in 1 BLISTER PACK

NDC Code 67046-208-21

Package Description: 21 CAPSULE in 1 BLISTER PACK

NDC Code 67046-208-28

Package Description: 28 CAPSULE in 1 BLISTER PACK

NDC Code 67046-208-30

Package Description: 30 CAPSULE in 1 BLISTER PACK

NDC Code 67046-208-60

Package Description: 60 CAPSULE in 1 BLISTER PACK

Product Details

What is NDC 67046-208?

The NDC code 67046-208 is assigned by the FDA to the product Prazosin Hydrochloride which is product labeled by Contract Pharmacy Services-pa. The product's dosage form is . The product is distributed in 8 packages with assigned NDC codes 67046-208-07 7 capsule in 1 blister pack , 67046-208-14 14 capsule in 1 blister pack , 67046-208-15 15 capsule in 1 blister pack , 67046-208-20 20 capsule in 1 blister pack , 67046-208-21 21 capsule in 1 blister pack , 67046-208-28 28 capsule in 1 blister pack , 67046-208-30 30 capsule in 1 blister pack , 67046-208-60 60 capsule in 1 blister pack . 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.

Which are Prazosin Hydrochloride UNII Codes?

The UNII codes for the active ingredients in this product are:

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:

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:

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Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".