NDC 17224-360 Diethylpropion Hydrochloride ER
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 17224 - Calvin, Scott And Company, Incorporated
- 17224-360 - Diethylpropion Hydrochloride
Product Characteristics
Product Packages
NDC Code 17224-360-10
Package Description: 28 TABLET, EXTENDED RELEASE in 1 BOTTLE
Product Details
What is NDC 17224-360?
What are the uses for Diethylpropion Hydrochloride ER?
Which are Diethylpropion Hydrochloride ER UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIETHYLPROPION HYDROCHLORIDE (UNII: 19V2PL39NG)
- DIETHYLPROPION (UNII: Q94YYU22B8) (Active Moiety)
Which are Diethylpropion Hydrochloride ER 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:
- MANNITOL (UNII: 3OWL53L36A)
- CARBOMER HOMOPOLYMER TYPE A (UNII: F68VH75CJC)
- TARTARIC ACID (UNII: W4888I119H)
- HYPROMELLOSE ACETATE SUCCINATE 06081224 (3 MM2/S) (UNII: 6N003M473W)
- POVIDONE K30 (UNII: U725QWY32X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
What is the NDC to RxNorm Crosswalk for Diethylpropion Hydrochloride ER?
- RxCUI: 978668 - diethylpropion HCl 75 MG 24HR Extended Release Oral Tablet
- RxCUI: 978668 - 24 HR diethylpropion hydrochloride 75 MG Extended Release Oral Tablet
- RxCUI: 978668 - diethylpropion hydrochloride 75 MG 24 HR Extended Release 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".