NDC 50436-3125 Omeprazole
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50436 - Unit Dose Services
- 50436-3125 - Omeprazole
Product Characteristics
YELLOW (C48330 - OPAQUE GOLD BODY)
Product Packages
NDC Code 50436-3125-1
Package Description: 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE
NDC Code 50436-3125-2
Package Description: 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE
NDC Code 50436-3125-3
Package Description: 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE
Product Details
What is NDC 50436-3125?
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, UNSPECIFIED (UNII: 2S7830E561)
- GLYCERYL DIBEHENATE (UNII: R8WTH25YS2)
- HYPROMELLOSE, UNSPECIFIED (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, UNSPECIFIED (UNII: 2G86QN327L)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- SHELLAC (UNII: 46N107B71O)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- AMMONIA (UNII: 5138Q19F1X)
- BUTYL ALCOHOL (UNII: 8PJ61P6TS3)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- ALUMINUM CHLOROHYDREX PROPYLENE GLYCOL (UNII: PGG6VG42HP)
- ALCOHOL (UNII: 3K9958V90M)
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
* Please review the disclaimer below.
Patient Education
Omeprazole
Prescription omeprazole is used alone or with other medications to treat the symptoms of gastroesophageal reflux disease (GERD), a condition in which backward flow of acid from the stomach causes heartburn and possible injury of the esophagus (the tube between the throat and stomach) in adults and children 1 year of age and older. Prescription omeprazole is used to treat damage from GERD in adults and children 1 month of age and older. Prescription omeprazole is used to allow the esophagus to heal and prevent further damage to the esophagus in adults and children 1 year of age and older with GERD. Prescription omeprazole is also used to treat conditions in which the stomach produces too much acid such as Zollinger-Ellison syndrome in adults. Prescription omeprazole is also used to treat ulcers (sores in the lining of the stomach or intestine) and it is also used with other medications to treat and prevent the return of ulcers caused by a certain type of bacteria (H. pylori) in adults. Nonprescription (over-the-counter) omeprazole is used to treat frequent heartburn (heartburn that occurs at least 2 or more days a week) in adults. Omeprazole is in a class of medications called proton-pump inhibitors. It works by decreasing the amount of acid made in the stomach.
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* 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".