NDC 42254-053 Omeprazole
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
18 MM
OMEPRAZOLE;20;MG;R;158
Product Packages
NDC Code 42254-053-07
Package Description: 7 CAPSULE, DELAYED RELEASE in 1 BOTTLE
NDC Code 42254-053-14
Package Description: 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE
NDC Code 42254-053-30
Package Description: 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE
NDC Code 42254-053-60
Package Description: 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE
NDC Code 42254-053-72
Package Description: 120 CAPSULE, DELAYED RELEASE in 1 BOTTLE
NDC Code 42254-053-90
Package Description: 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE
Product Details
What is NDC 42254-053?
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)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- MANNITOL (UNII: 3OWL53L36A)
- MEGLUMINE (UNII: 6HG8UB2MUY)
- METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A (UNII: NX76LV5T8J)
- POLOXAMER 124 (UNII: 1S66E28KXA)
- POVIDONE (UNII: FZ989GH94E)
- TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
- D&C RED NO. 28 (UNII: 767IP0Y5NH)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- GELATIN (UNII: 2G86QN327L)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- BUTYL ALCOHOL (UNII: 8PJ61P6TS3)
- SHELLAC (UNII: 46N107B71O)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- ALCOHOL (UNII: 3K9958V90M)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
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
* 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".