NDC 12634-118 Benzphetamine Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 12634 - Apotheca Inc.
- 12634-118 - Benzphetamine Hydrochloride
- 12634-118-00
- 12634-118-01
- 12634-118-09
- 12634-118-12
- 12634-118-18
- 12634-118-40
- 12634-118-42
- 12634-118-45
- 12634-118-50
- 12634-118-52
- 12634-118-54
- 12634-118-57
- 12634-118-59
- 12634-118-60
- 12634-118-61
- 12634-118-63
- 12634-118-66
- 12634-118-67
- 12634-118-69
- 12634-118-71
- 12634-118-74
- 12634-118-78
- 12634-118-79
- 12634-118-80
- 12634-118-81
- 12634-118-82
- 12634-118-84
- 12634-118-85
- 12634-118-90
- 12634-118-91
- 12634-118-92
- 12634-118-93
- 12634-118-94
- 12634-118-95
- 12634-118-96
- 12634-118-97
- 12634-118-98
- 12634-118-99
- 12634-118 - Benzphetamine Hydrochloride
Product Characteristics
Product Packages
NDC Code 12634-118-00
Package Description: 10 TABLET in 1 BOTTLE
NDC Code 12634-118-01
Package Description: 100 TABLET in 1 BOTTLE
NDC Code 12634-118-09
Package Description: 35 TABLET in 1 BOTTLE
NDC Code 12634-118-12
Package Description: 120 TABLET in 1 BOTTLE
NDC Code 12634-118-18
Package Description: 180 TABLET in 1 BOTTLE
NDC Code 12634-118-40
Package Description: 40 TABLET in 1 BOTTLE
NDC Code 12634-118-42
Package Description: 42 TABLET in 1 BOTTLE
NDC Code 12634-118-45
Package Description: 45 TABLET in 1 BOTTLE
NDC Code 12634-118-50
Package Description: 50 TABLET in 1 BOTTLE
NDC Code 12634-118-52
Package Description: 12 TABLET in 1 BLISTER PACK
NDC Code 12634-118-54
Package Description: 14 TABLET in 1 BLISTER PACK
NDC Code 12634-118-57
Package Description: 20 TABLET in 1 BLISTER PACK
NDC Code 12634-118-59
Package Description: 30 TABLET in 1 BLISTER PACK
NDC Code 12634-118-60
Package Description: 60 TABLET in 1 BOTTLE
NDC Code 12634-118-61
Package Description: 10 TABLET in 1 BLISTER PACK
NDC Code 12634-118-63
Package Description: 3 TABLET in 1 BLISTER PACK
NDC Code 12634-118-66
Package Description: 6 TABLET in 1 BLISTER PACK
NDC Code 12634-118-67
Package Description: 7 TABLET in 1 BLISTER PACK
NDC Code 12634-118-69
Package Description: 9 TABLET in 1 BLISTER PACK
NDC Code 12634-118-71
Package Description: 30 TABLET in 1 BOTTLE
NDC Code 12634-118-74
Package Description: 24 TABLET in 1 BOTTLE
NDC Code 12634-118-78
Package Description: 28 TABLET in 1 BOTTLE
NDC Code 12634-118-79
Package Description: 25 TABLET in 1 BOTTLE
NDC Code 12634-118-80
Package Description: 20 TABLET in 1 BOTTLE
NDC Code 12634-118-81
Package Description: 21 TABLET in 1 BOTTLE
NDC Code 12634-118-82
Package Description: 12 TABLET in 1 BOTTLE
NDC Code 12634-118-84
Package Description: 14 TABLET in 1 BOTTLE
NDC Code 12634-118-85
Package Description: 15 TABLET in 1 BOTTLE
NDC Code 12634-118-90
Package Description: 90 TABLET in 1 BOTTLE
NDC Code 12634-118-91
Package Description: 1 TABLET in 1 BLISTER PACK
NDC Code 12634-118-92
Package Description: 2 TABLET in 1 BOTTLE
NDC Code 12634-118-93
Package Description: 3 TABLET in 1 BOTTLE
NDC Code 12634-118-94
Package Description: 4 TABLET in 1 BOTTLE
NDC Code 12634-118-95
Package Description: 95 TABLET in 1 BOTTLE
NDC Code 12634-118-96
Package Description: 6 TABLET in 1 BOTTLE
NDC Code 12634-118-97
Package Description: 7 TABLET in 1 BOTTLE
NDC Code 12634-118-98
Package Description: 8 TABLET in 1 BOTTLE
NDC Code 12634-118-99
Package Description: 9 TABLET in 1 BOTTLE
Product Details
What is NDC 12634-118?
What are the uses for Benzphetamine Hydrochloride?
Which are Benzphetamine Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZPHETAMINE HYDROCHLORIDE (UNII: 43DWT87QT7)
- BENZPHETAMINE (UNII: 0M3S43XK27) (Active Moiety)
Which are Benzphetamine 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:
- CALCIUM STEARATE (UNII: 776XM7047L)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- LACTOSE (UNII: J2B2A4N98G)
- POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P)
- SORBITOL (UNII: 506T60A25R)
What is the NDC to RxNorm Crosswalk for Benzphetamine Hydrochloride?
- RxCUI: 904368 - benzphetamine HCl 50 MG Oral Tablet
- RxCUI: 904368 - benzphetamine hydrochloride 50 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".