NDC 54868-3071 Phendimetrazine Tartrate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-3071 - Phendimetrazine Tartrate
Product Characteristics
Product Packages
NDC Code 54868-3071-0
Package Description: 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE
NDC Code 54868-3071-1
Package Description: 7 CAPSULE, EXTENDED RELEASE in 1 BOTTLE
NDC Code 54868-3071-2
Package Description: 10 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
Product Details
What is NDC 54868-3071?
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:
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- GELATIN (UNII: 2G86QN327L)
- POVIDONE (UNII: FZ989GH94E)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- STARCH, CORN (UNII: O8232NY3SJ)
- SUCROSE (UNII: C151H8M554)
- TALC (UNII: 7SEV7J4R1U)
- SHELLAC (UNII: 46N107B71O)
What is the NDC to RxNorm Crosswalk for Phendimetrazine Tartrate?
- RxCUI: 979543 - phendimetrazine tartrate 105 MG 24HR Extended Release Oral Capsule
- RxCUI: 979543 - 24 HR phendimetrazine tartrate 105 MG Extended Release Oral Capsule
- RxCUI: 979543 - phendimetrazine 105 MG 24 HR Extended Release Oral Capsule
* 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".