NDC 54868-5303 Prevacid
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-5303 - Prevacid
Product Characteristics
PINK (C48328 - OPAQUE, HARD GELATIN COLORED PINK AND BLACK)
WHITE (C48325 - WHITE TO YELLOWISH WHITE UNCOATED TABLETS WITH ORANGE TO DARK BROWN SPECKLES)
ROUND (C48348)
19 MM
9 MM
12 MM
TAP;PREVACID;30
15
30
Product Packages
NDC Code 54868-5303-0
Package Description: 30 TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE in 1 BOTTLE
NDC Code 54868-5303-1
Package Description: 10 TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE in 1 BOTTLE
Product Details
What is NDC 54868-5303?
What are the uses for Prevacid?
Which are Prevacid UNII Codes?
The UNII codes for the active ingredients in this product are:
- LANSOPRAZOLE (UNII: 0K5C5T2QPG)
- LANSOPRAZOLE (UNII: 0K5C5T2QPG) (Active Moiety)
Which are Prevacid 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)
- METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A (UNII: NX76LV5T8J)
- 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)
- MANNITOL (UNII: 3OWL53L36A)
- METHACRYLIC ACID (UNII: 1CS02G8656)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
- CROSPOVIDONE (UNII: 68401960MK)
- ASPARTAME (UNII: Z0H242BBR1)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- PHENYLALANINE (UNII: 47E5O17Y3R)
What is the NDC to RxNorm Crosswalk for Prevacid?
- RxCUI: 206205 - Prevacid SoluTab 15 MG Delayed Release Disintegrating Oral Tablet
- RxCUI: 206205 - lansoprazole 15 MG Disintegrating Oral Tablet [Prevacid]
- RxCUI: 206205 - Prevacid 15 MG Delayed Release Disintegrating Oral Tablet
- RxCUI: 206206 - Prevacid 30 MG Delayed Release Oral Capsule
- RxCUI: 206206 - lansoprazole 30 MG Delayed Release Oral Capsule [Prevacid]
* 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".