NDC 12634-605 Atenolol

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.

Product Characteristics

Color(s):
WHITE (C48325 - WHITE TO OFF- WHITE)
Shape:
ROUND (C48348)
Size(s):
10 MM
Imprint(s):
Z;67
Score:
1

Product Packages

NDC Code 12634-605-00

Package Description: 10 TABLET in 1 BOTTLE

NDC Code 12634-605-01

Package Description: 100 TABLET in 1 BOTTLE

NDC Code 12634-605-09

Package Description: 35 TABLET in 1 BOTTLE

NDC Code 12634-605-40

Package Description: 40 TABLET in 1 BOTTLE

NDC Code 12634-605-42

Package Description: 42 TABLET in 1 BOTTLE

NDC Code 12634-605-45

Package Description: 45 TABLET in 1 BOTTLE

NDC Code 12634-605-50

Package Description: 50 TABLET in 1 BOTTLE

NDC Code 12634-605-52

Package Description: 12 TABLET in 1 BLISTER PACK

NDC Code 12634-605-54

Package Description: 14 TABLET in 1 BLISTER PACK

NDC Code 12634-605-57

Package Description: 20 TABLET in 1 BLISTER PACK

NDC Code 12634-605-58

Package Description: 28 TABLET in 1 BLISTER PACK

NDC Code 12634-605-59

Package Description: 30 TABLET in 1 BLISTER PACK

NDC Code 12634-605-60

Package Description: 60 TABLET in 1 BOTTLE

NDC Code 12634-605-61

Package Description: 10 TABLET in 1 BLISTER PACK

NDC Code 12634-605-63

Package Description: 3 TABLET in 1 BLISTER PACK

NDC Code 12634-605-66

Package Description: 6 TABLET in 1 BLISTER PACK

NDC Code 12634-605-67

Package Description: 7 TABLET in 1 BLISTER PACK

NDC Code 12634-605-69

Package Description: 9 TABLET in 1 BLISTER PACK

NDC Code 12634-605-71

Package Description: 30 TABLET in 1 BOTTLE

NDC Code 12634-605-74

Package Description: 24 TABLET in 1 BOTTLE

NDC Code 12634-605-78

Package Description: 28 TABLET in 1 BOTTLE

NDC Code 12634-605-79

Package Description: 25 TABLET in 1 BOTTLE

NDC Code 12634-605-80

Package Description: 20 TABLET in 1 BOTTLE

NDC Code 12634-605-81

Package Description: 21 TABLET in 1 BOTTLE

NDC Code 12634-605-82

Package Description: 12 TABLET in 1 BOTTLE

NDC Code 12634-605-84

Package Description: 14 TABLET in 1 BOTTLE

NDC Code 12634-605-85

Package Description: 15 TABLET in 1 BOTTLE

NDC Code 12634-605-90

Package Description: 90 TABLET in 1 BOTTLE

NDC Code 12634-605-91

Package Description: 1 TABLET in 1 BLISTER PACK

NDC Code 12634-605-92

Package Description: 2 TABLET in 1 BOTTLE

NDC Code 12634-605-93

Package Description: 3 TABLET in 1 BOTTLE

NDC Code 12634-605-94

Package Description: 4 TABLET in 1 BOTTLE

NDC Code 12634-605-95

Package Description: 5 TABLET in 1 BOTTLE

NDC Code 12634-605-96

Package Description: 6 TABLET in 1 BOTTLE

NDC Code 12634-605-97

Package Description: 7 TABLET in 1 BOTTLE

NDC Code 12634-605-98

Package Description: 8 TABLET in 1 BOTTLE

NDC Code 12634-605-99

Package Description: 9 TABLET in 1 BOTTLE

Product Details

What is NDC 12634-605?

The NDC code 12634-605 is assigned by the FDA to the product Atenolol which is product labeled by Apotheca Inc.. The product's dosage form is . The product is distributed in 37 packages with assigned NDC codes 12634-605-00 10 tablet in 1 bottle , 12634-605-01 100 tablet in 1 bottle , 12634-605-09 35 tablet in 1 bottle , 12634-605-40 40 tablet in 1 bottle , 12634-605-42 42 tablet in 1 bottle , 12634-605-45 45 tablet in 1 bottle , 12634-605-50 50 tablet in 1 bottle , 12634-605-52 12 tablet in 1 blister pack , 12634-605-54 14 tablet in 1 blister pack , 12634-605-57 20 tablet in 1 blister pack , 12634-605-58 28 tablet in 1 blister pack , 12634-605-59 30 tablet in 1 blister pack , 12634-605-60 60 tablet in 1 bottle , 12634-605-61 10 tablet in 1 blister pack , 12634-605-63 3 tablet in 1 blister pack , 12634-605-66 6 tablet in 1 blister pack , 12634-605-67 7 tablet in 1 blister pack , 12634-605-69 9 tablet in 1 blister pack , 12634-605-71 30 tablet in 1 bottle , 12634-605-74 24 tablet in 1 bottle , 12634-605-78 28 tablet in 1 bottle , 12634-605-79 25 tablet in 1 bottle , 12634-605-80 20 tablet in 1 bottle , 12634-605-81 21 tablet in 1 bottle , 12634-605-82 12 tablet in 1 bottle , 12634-605-84 14 tablet in 1 bottle , 12634-605-85 15 tablet in 1 bottle , 12634-605-90 90 tablet in 1 bottle , 12634-605-91 1 tablet in 1 blister pack , 12634-605-92 2 tablet in 1 bottle , 12634-605-93 3 tablet in 1 bottle , 12634-605-94 4 tablet in 1 bottle , 12634-605-95 5 tablet in 1 bottle , 12634-605-96 6 tablet in 1 bottle , 12634-605-97 7 tablet in 1 bottle , 12634-605-98 8 tablet in 1 bottle , 12634-605-99 9 tablet 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 Atenolol?

Atenolol is used with or without other medications to treat high blood pressure (hypertension). Lowering high blood pressure helps prevent strokes, heart attacks, and kidney problems. This medication is also used to treat chest pain (angina) and to improve survival after a heart attack. Atenolol belongs to a class of drugs known as beta blockers. It works by blocking the action of certain natural chemicals in your body, such as epinephrine, on the heart and blood vessels. This effect lowers the heart rate, blood pressure, and strain on the heart.

Which are Atenolol UNII Codes?

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

Which are Atenolol 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 Atenolol?

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 code indicates a single concept unique identifier (RXCUI) is 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".