NDC 16853-1308 Omesec
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 16853 - Corporacion Infarmasa
- 16853-1308 - Omesec
Product Characteristics
Product Packages
NDC Code 16853-1308-1
Package Description: 14 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK
NDC Code 16853-1308-2
Package Description: 28 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK
NDC Code 16853-1308-3
Package Description: 42 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK
NDC Code 16853-1308-4
Package Description: 2 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK
Product Details
What is NDC 16853-1308?
What are the uses for Omesec?
Which are Omesec UNII Codes?
The UNII codes for the active ingredients in this product are:
- OMEPRAZOLE (UNII: KG60484QX9)
- OMEPRAZOLE (UNII: KG60484QX9) (Active Moiety)
Which are Omesec 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:
- DIETHYL PHTHALATE (UNII: UF064M00AF)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- SODIUM PHOSPHATE, DIBASIC, DIHYDRATE (UNII: 94255I6E2T)
- HYDROXYPROPYL CELLULOSE (UNII: RFW2ET671P)
- LACTOSE (UNII: J2B2A4N98G)
- HYPROMELLOSE (UNII: 3NXW29V3WO)
- STARCH, CORN (UNII: O8232NY3SJ)
- HYPROMELLOSE PHTHALATE (31% PHTHALATE, 170 CST) (UNII: 8LDD2V82F5)
- SUCROSE (UNII: C151H8M554)
What is the NDC to RxNorm Crosswalk for Omesec?
- 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: 967525 - omeprazole 20 MG Delayed Release Oral Capsule [Omesec]
- RxCUI: 967525 - Omesec 20 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".