NDC 54868-5911 Omeprazole
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-5911 - Omeprazole
Product Characteristics
Product Packages
NDC Code 54868-5911-0
Package Description: 6 BLISTER PACK in 1 CARTON / 7 TABLET, DELAYED RELEASE in 1 BLISTER PACK
Product Details
What is NDC 54868-5911?
What are the uses for Omeprazole?
Which are Omeprazole UNII Codes?
The UNII codes for the active ingredients in this product are:
- OMEPRAZOLE (UNII: KG60484QX9)
- OMEPRAZOLE (UNII: KG60484QX9) (Active Moiety)
Which are Omeprazole 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)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- HYPROMELLOSE (UNII: 3NXW29V3WO)
- HYPROMELLOSE ACETATE SUCCINATE 12070923 (3 MM2/S) (UNII: 36BGF0E889)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- ETHANOLAMINE (UNII: 5KV86114PT)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- SODIUM STEARATE (UNII: QU7E2XA9TG)
- SODIUM STEARYL FUMARATE (UNII: 7CV7WJK4UI)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
What is the NDC to RxNorm Crosswalk for Omeprazole?
- RxCUI: 402014 - omeprazole 20 MG Delayed Release Oral Tablet
- RxCUI: 402014 - omeprazole 20 MG (as omeprazole magnesium 20.6 MG) Delayed 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".