NDC 68387-696 Diethylpropion Hcl Controlled-release
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
OVAL (C48345)
19 MM
WATSON;782
Code Structure Chart
Product Details
What is NDC 68387-696?
What are the uses for Diethylpropion Hcl Controlled-release?
Which are Diethylpropion Hcl Controlled-release 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 Hcl Controlled-release 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:
- STARCH, CORN (UNII: O8232NY3SJ)
- LACTOSE (UNII: J2B2A4N98G)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- TALC (UNII: 7SEV7J4R1U)
- TARTARIC ACID (UNII: W4888I119H)
- CARBOMER 934 (UNII: Z135WT9208)
- MANNITOL (UNII: 3OWL53L36A)
- POVIDONE (UNII: FZ989GH94E)
- ZINC STEARATE (UNII: H92E6QA4FV)
What is the NDC to RxNorm Crosswalk for Diethylpropion Hcl Controlled-release?
- RxCUI: 978654 - diethylpropion HCl 25 MG Oral Tablet
- RxCUI: 978654 - diethylpropion hydrochloride 25 MG Oral Tablet
- 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".