NDC 68151-4488 Strattera
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68151 - Carilion Materials Management
- 68151-4488 - Strattera
Product Characteristics
YELLOW (C48330 - GOLD)
Product Packages
NDC Code 68151-4488-3
Package Description: 1 CAPSULE in 1 PACKAGE
Product Details
What is NDC 68151-4488?
What are the uses for Strattera?
Which are Strattera UNII Codes?
The UNII codes for the active ingredients in this product are:
- ATOMOXETINE HYDROCHLORIDE (UNII: 57WVB6I2W0)
- ATOMOXETINE (UNII: ASW034S0B8) (Active Moiety)
Which are Strattera 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)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- GELATIN (UNII: 2G86QN327L)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Strattera?
- RxCUI: 349595 - atomoxetine HCl 60 MG Oral Capsule
- RxCUI: 349595 - atomoxetine 60 MG Oral Capsule
- RxCUI: 349595 - atomoxetine 60 MG (as atomoxetine hydrochloride) Oral Capsule
- RxCUI: 352321 - Strattera 60 MG Oral Capsule
- RxCUI: 352321 - atomoxetine 60 MG Oral Capsule [Strattera]
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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".