NDC 54868-3941 Zyprexa
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-3941 - Zyprexa
Product Characteristics
8 MM
9 MM
10 MM
LILLY;4115
LILLY;4116
LILLY;4117
Product Packages
NDC Code 54868-3941-0
Package Description: 30 TABLET in 1 BOTTLE
Product Details
What is NDC 54868-3941?
What are the uses for Zyprexa?
Which are Zyprexa UNII Codes?
The UNII codes for the active ingredients in this product are:
- OLANZAPINE (UNII: N7U69T4SZR)
- OLANZAPINE (UNII: N7U69T4SZR) (Active Moiety)
Which are Zyprexa 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:
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- CROSPOVIDONE (UNII: 68401960MK)
- HYDROXYPROPYL CELLULOSE (UNII: RFW2ET671P)
- HYPROMELLOSE (UNII: 3NXW29V3WO)
- LACTOSE (UNII: J2B2A4N98G)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
What is the NDC to RxNorm Crosswalk for Zyprexa?
- RxCUI: 153046 - ZyPREXA 5 MG Oral Tablet
- RxCUI: 153046 - olanzapine 5 MG Oral Tablet [Zyprexa]
- RxCUI: 153046 - Zyprexa 5 MG Oral Tablet
- RxCUI: 153047 - ZyPREXA 7.5 MG Oral Tablet
- RxCUI: 153047 - olanzapine 7.5 MG Oral Tablet [Zyprexa]
* 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".