NDC 21695-652 Lansoprazole
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 21695 - Rebel Distributors Corp
- 21695-652 - Lansoprazole
Product Characteristics
PINK (C48328 - OPAQUE)
BLACK (C48323 - OPAQUE)
19 MM
TAP;PREVACID;30
Product Packages
NDC Code 21695-652-30
Package Description: 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE
Product Details
What is NDC 21695-652?
What are the uses for Lansoprazole?
Which are Lansoprazole UNII Codes?
The UNII codes for the active ingredients in this product are:
- LANSOPRAZOLE (UNII: 0K5C5T2QPG)
- LANSOPRAZOLE (UNII: 0K5C5T2QPG) (Active Moiety)
Which are Lansoprazole 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:
- STARCH, CORN (UNII: O8232NY3SJ)
- SUCROSE (UNII: C151H8M554)
- HYDROXYPROPYL CELLULOSE, LOW SUBSTITUTED (UNII: 2165RE0K14)
- MAGNESIUM CARBONATE (UNII: 0E53J927NA)
- TALC (UNII: 7SEV7J4R1U)
- POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- HYDROXYPROPYL CELLULOSE (UNII: RFW2ET671P)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- D&C RED NO. 28 (UNII: 767IP0Y5NH)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A (UNII: NX76LV5T8J)
What is the NDC to RxNorm Crosswalk for Lansoprazole?
- RxCUI: 311277 - lansoprazole 30 MG Delayed Release Oral Capsule
- RxCUI: 596843 - lansoprazole 15 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".