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  4. NDC Product Code: 21695-106 Prevacid Solutab

NDC 21695-106 Prevacid Solutab

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 21695-106?
  5. Prevacid Solutab Uses
  6. Active Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
21695-106
Proprietary Name:
Prevacid Solutab
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Rebel Distributors Corp
Labeler Code:
21695
Product Label ID:
d15c8f36-4dcc-4b28-b03c-4e81b2f9ad2e
Start Marketing Date: [9]
08-30-2002
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - WHITE TO YELLOWISH WHITE UNCOATED TABLETS WITH ORANGE TO DARK BROWN SPECKLES)
Shape:
ROUND (C48348)
Size(s):
12 MM
Imprint(s):
30
Score:
1
Flavor(s):
STRAWBERRY (C73417 - ARTIFICIAL STRAWBERRY FLAVOR)

Code Structure Chart

Product Details

What is NDC 21695-106?

The NDC code 21695-106 is assigned by the FDA to the product Prevacid Solutab which is product labeled by Rebel Distributors Corp. The product's dosage form is . The product is distributed in a single package with assigned NDC code 21695-106-15 15 tablet, orally disintegrating, delayed release in 1 bottle . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Prevacid Solutab?

PREVACID is contraindicated in patients with known severe hypersensitivity to any component of the formulation of PREVACID. For information on contraindications for amoxicillin or clarithromycin, refer to their full prescribing information, CONTRAINDICATIONS sections.

Which are Prevacid Solutab UNII Codes?

The UNII codes for the active ingredients in this product are:

* Please review the disclaimer below.

Product Footnotes

[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".