NDC 54868-5987 Omeprazole
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-5987 - Omeprazole
Product Characteristics
WHITE (C48325 - OPAQUE WHITE BODY)
YELLOW (C48330 - OPAQUE GOLD BODY)
YELLOW (C48330 - OPAQUE GOLD CAP)
19 MM
22 MM
KU;118
KU;136
Product Packages
NDC Code 54868-5987-0
Package Description: 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE
NDC Code 54868-5987-1
Package Description: 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE
NDC Code 54868-5987-2
Package Description: 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE
Product Details
What is NDC 54868-5987?
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:
- CROSPOVIDONE (UNII: 68401960MK)
- GLYCERYL DIBEHENATE (UNII: R8WTH25YS2)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1) (UNII: 74G4R6TH13)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
- GELATIN (UNII: 2G86QN327L)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- SHELLAC (UNII: 46N107B71O)
- AMMONIA (UNII: 5138Q19F1X)
- BUTYL ALCOHOL (UNII: 8PJ61P6TS3)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- ALUMINUM CHLOROHYDREX PROPYLENE GLYCOL (UNII: PGG6VG42HP)
- ALCOHOL (UNII: 3K9958V90M)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
What is the NDC to RxNorm Crosswalk for Omeprazole?
- RxCUI: 198051 - omeprazole 20 MG Delayed Release Oral Capsule
- RxCUI: 198051 - omeprazole 20 MG (as omeprazole magnesium 20.6 MG) Delayed Release Oral Capsule
- RxCUI: 199119 - omeprazole 10 MG Delayed Release Oral Capsule
- RxCUI: 199119 - omeprazole (as omeprazole magnesium) 10 MG Delayed Release Oral Capsule
- RxCUI: 200329 - omeprazole 40 MG Delayed Release Oral Capsule
* 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".