NDC 12634-539 Phendimetrazine Tartrate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 12634 - Apotheca Inc.
- 12634-539 - Phendimetrazine Tartrate
- 12634-539-00
- 12634-539-01
- 12634-539-09
- 12634-539-40
- 12634-539-42
- 12634-539-45
- 12634-539-50
- 12634-539-52
- 12634-539-54
- 12634-539-57
- 12634-539-58
- 12634-539-59
- 12634-539-60
- 12634-539-61
- 12634-539-63
- 12634-539-66
- 12634-539-67
- 12634-539-69
- 12634-539-71
- 12634-539-74
- 12634-539-78
- 12634-539-79
- 12634-539-80
- 12634-539-81
- 12634-539-82
- 12634-539-84
- 12634-539-85
- 12634-539-90
- 12634-539-91
- 12634-539-92
- 12634-539-93
- 12634-539-94
- 12634-539-95
- 12634-539-96
- 12634-539-97
- 12634-539-98
- 12634-539-99
- 12634-539 - Phendimetrazine Tartrate
Product Characteristics
Product Packages
NDC Code 12634-539-00
Package Description: 10 TABLET in 1 BOTTLE
NDC Code 12634-539-01
Package Description: 100 TABLET in 1 BOTTLE
NDC Code 12634-539-09
Package Description: 35 TABLET in 1 BOTTLE
NDC Code 12634-539-40
Package Description: 40 TABLET in 1 BOTTLE
NDC Code 12634-539-42
Package Description: 42 TABLET in 1 BOTTLE
NDC Code 12634-539-45
Package Description: 45 TABLET in 1 BOTTLE
NDC Code 12634-539-50
Package Description: 50 TABLET in 1 BOTTLE
NDC Code 12634-539-52
Package Description: 12 TABLET in 1 BLISTER PACK
NDC Code 12634-539-54
Package Description: 14 TABLET in 1 BLISTER PACK
NDC Code 12634-539-57
Package Description: 20 TABLET in 1 BLISTER PACK
NDC Code 12634-539-58
Package Description: 28 TABLET in 1 BLISTER PACK
NDC Code 12634-539-59
Package Description: 30 TABLET in 1 BLISTER PACK
NDC Code 12634-539-60
Package Description: 60 TABLET in 1 BOTTLE
NDC Code 12634-539-61
Package Description: 10 TABLET in 1 BLISTER PACK
NDC Code 12634-539-63
Package Description: 3 TABLET in 1 BLISTER PACK
NDC Code 12634-539-66
Package Description: 6 TABLET in 1 BLISTER PACK
NDC Code 12634-539-67
Package Description: 7 TABLET in 1 BLISTER PACK
NDC Code 12634-539-69
Package Description: 9 TABLET in 1 BLISTER PACK
NDC Code 12634-539-71
Package Description: 30 TABLET in 1 BOTTLE
NDC Code 12634-539-74
Package Description: 24 TABLET in 1 BOTTLE
NDC Code 12634-539-78
Package Description: 28 TABLET in 1 BOTTLE
NDC Code 12634-539-79
Package Description: 25 TABLET in 1 BOTTLE
NDC Code 12634-539-80
Package Description: 20 TABLET in 1 BOTTLE
NDC Code 12634-539-81
Package Description: 21 TABLET in 1 BOTTLE
NDC Code 12634-539-82
Package Description: 12 TABLET in 1 BOTTLE
NDC Code 12634-539-84
Package Description: 14 TABLET in 1 BOTTLE
NDC Code 12634-539-85
Package Description: 15 TABLET in 1 BOTTLE
NDC Code 12634-539-90
Package Description: 90 TABLET in 1 BOTTLE
NDC Code 12634-539-91
Package Description: 1 TABLET in 1 BLISTER PACK
NDC Code 12634-539-92
Package Description: 2 TABLET in 1 BOTTLE
NDC Code 12634-539-93
Package Description: 3 TABLET in 1 BOTTLE
NDC Code 12634-539-94
Package Description: 4 TABLET in 1 BOTTLE
NDC Code 12634-539-95
Package Description: 5 TABLET in 1 BOTTLE
NDC Code 12634-539-96
Package Description: 6 TABLET in 1 BOTTLE
NDC Code 12634-539-97
Package Description: 7 TABLET in 1 BOTTLE
NDC Code 12634-539-98
Package Description: 8 TABLET in 1 BOTTLE
NDC Code 12634-539-99
Package Description: 9 TABLET in 1 BOTTLE
Product Details
What is NDC 12634-539?
What are the uses for Phendimetrazine Tartrate?
Which are Phendimetrazine Tartrate UNII Codes?
The UNII codes for the active ingredients in this product are:
- PHENDIMETRAZINE TARTRATE (UNII: 6985IP0T80)
- PHENDIMETRAZINE (UNII: AB2794W8KV) (Active Moiety)
Which are Phendimetrazine Tartrate 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 PHOSPHATE, DIBASIC, DIHYDRATE (UNII: O7TSZ97GEP)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
What is the NDC to RxNorm Crosswalk for Phendimetrazine Tartrate?
- RxCUI: 979549 - phendimetrazine tartrate 35 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".