NDC 12634-605 Atenolol
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 12634 - Apotheca Inc.
- 12634-605 - Atenolol
- 12634-605-00
- 12634-605-01
- 12634-605-09
- 12634-605-40
- 12634-605-42
- 12634-605-45
- 12634-605-50
- 12634-605-52
- 12634-605-54
- 12634-605-57
- 12634-605-58
- 12634-605-59
- 12634-605-60
- 12634-605-61
- 12634-605-63
- 12634-605-66
- 12634-605-67
- 12634-605-69
- 12634-605-71
- 12634-605-74
- 12634-605-78
- 12634-605-79
- 12634-605-80
- 12634-605-81
- 12634-605-82
- 12634-605-84
- 12634-605-85
- 12634-605-90
- 12634-605-91
- 12634-605-92
- 12634-605-93
- 12634-605-94
- 12634-605-95
- 12634-605-96
- 12634-605-97
- 12634-605-98
- 12634-605-99
- 12634-605 - Atenolol
Product Characteristics
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?
What are the uses for Atenolol?
Which are Atenolol UNII Codes?
The UNII codes for the active ingredients in this product are:
- ATENOLOL (UNII: 50VV3VW0TI)
- ATENOLOL (UNII: 50VV3VW0TI) (Active Moiety)
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:
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- POVIDONE (UNII: FZ989GH94E)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
What is the NDC to RxNorm Crosswalk for Atenolol?
- RxCUI: 197379 - atenolol 100 MG Oral Tablet
* Please review the disclaimer below.
[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".