NDC 12634-600 Amlodipine Besylate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 12634 - Apotheca Inc.
- 12634-600 - Amlodipine Besylate
- 12634-600-00
- 12634-600-01
- 12634-600-09
- 12634-600-40
- 12634-600-42
- 12634-600-45
- 12634-600-50
- 12634-600-52
- 12634-600-54
- 12634-600-57
- 12634-600-58
- 12634-600-59
- 12634-600-60
- 12634-600-61
- 12634-600-63
- 12634-600-66
- 12634-600-67
- 12634-600-69
- 12634-600-71
- 12634-600-74
- 12634-600-78
- 12634-600-79
- 12634-600-80
- 12634-600-81
- 12634-600-82
- 12634-600-84
- 12634-600-85
- 12634-600-90
- 12634-600-91
- 12634-600-92
- 12634-600-93
- 12634-600-94
- 12634-600-95
- 12634-600-96
- 12634-600-97
- 12634-600-98
- 12634-600-99
- 12634-600 - Amlodipine Besylate
Product Characteristics
Product Packages
NDC Code 12634-600-00
Package Description: 10 TABLET in 1 BOTTLE
NDC Code 12634-600-01
Package Description: 100 TABLET in 1 BOTTLE
NDC Code 12634-600-09
Package Description: 35 TABLET in 1 BOTTLE
NDC Code 12634-600-40
Package Description: 40 TABLET in 1 BOTTLE
NDC Code 12634-600-42
Package Description: 42 TABLET in 1 BOTTLE
NDC Code 12634-600-45
Package Description: 45 TABLET in 1 BOTTLE
NDC Code 12634-600-50
Package Description: 50 TABLET in 1 BOTTLE
NDC Code 12634-600-52
Package Description: 12 TABLET in 1 BLISTER PACK
NDC Code 12634-600-54
Package Description: 14 TABLET in 1 BLISTER PACK
NDC Code 12634-600-57
Package Description: 20 TABLET in 1 BLISTER PACK
NDC Code 12634-600-58
Package Description: 28 TABLET in 1 BLISTER PACK
NDC Code 12634-600-59
Package Description: 30 TABLET in 1 BLISTER PACK
NDC Code 12634-600-60
Package Description: 60 TABLET in 1 BOTTLE
NDC Code 12634-600-61
Package Description: 10 TABLET in 1 BLISTER PACK
NDC Code 12634-600-63
Package Description: 3 TABLET in 1 BLISTER PACK
NDC Code 12634-600-66
Package Description: 6 TABLET in 1 BLISTER PACK
NDC Code 12634-600-67
Package Description: 7 TABLET in 1 BLISTER PACK
NDC Code 12634-600-69
Package Description: 9 TABLET in 1 BLISTER PACK
NDC Code 12634-600-71
Package Description: 30 TABLET in 1 BOTTLE
NDC Code 12634-600-74
Package Description: 24 TABLET in 1 BOTTLE
NDC Code 12634-600-78
Package Description: 28 TABLET in 1 BOTTLE
NDC Code 12634-600-79
Package Description: 25 TABLET in 1 BOTTLE
NDC Code 12634-600-80
Package Description: 20 TABLET in 1 BOTTLE
NDC Code 12634-600-81
Package Description: 21 TABLET in 1 BOTTLE
NDC Code 12634-600-82
Package Description: 12 TABLET in 1 BOTTLE
NDC Code 12634-600-84
Package Description: 14 TABLET in 1 BOTTLE
NDC Code 12634-600-85
Package Description: 15 TABLET in 1 BOTTLE
NDC Code 12634-600-90
Package Description: 90 TABLET in 1 BOTTLE
NDC Code 12634-600-91
Package Description: 1 TABLET in 1 BLISTER PACK
NDC Code 12634-600-92
Package Description: 2 TABLET in 1 BOTTLE
NDC Code 12634-600-93
Package Description: 3 TABLET in 1 BOTTLE
NDC Code 12634-600-94
Package Description: 4 TABLET in 1 BOTTLE
NDC Code 12634-600-95
Package Description: 5 TABLET in 1 BOTTLE
NDC Code 12634-600-96
Package Description: 6 TABLET in 1 BOTTLE
NDC Code 12634-600-97
Package Description: 7 TABLET in 1 BOTTLE
NDC Code 12634-600-98
Package Description: 8 TABLET in 1 BOTTLE
NDC Code 12634-600-99
Package Description: 9 TABLET in 1 BOTTLE
Product Details
What is NDC 12634-600?
What are the uses for Amlodipine Besylate?
Which are Amlodipine Besylate UNII Codes?
The UNII codes for the active ingredients in this product are:
- AMLODIPINE BESYLATE (UNII: 864V2Q084H)
- AMLODIPINE (UNII: 1J444QC288) (Active Moiety)
Which are Amlodipine Besylate 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:
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- ANHYDROUS DIBASIC CALCIUM PHOSPHATE (UNII: L11K75P92J)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
What is the NDC to RxNorm Crosswalk for Amlodipine Besylate?
- RxCUI: 308135 - amLODIPine besylate 10 MG Oral Tablet
- RxCUI: 308135 - amlodipine 10 MG Oral Tablet
- RxCUI: 308135 - amlodipine (as amlodipine besylate) 10 MG Oral Tablet
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[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".