Label: CONTRAST ALLERGY PREMED PACK- prednisone, diphenhydramine kit
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Contains inactivated NDC Code(s)
NDC Code(s): 16129-101-01 - Packager: Shertech Laboratories, LLC
- Category: HUMAN PRESCRIPTION DRUG LABEL
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated March 13, 2018
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- DESCRIPTION
- Contrast Allergy PreMed Pack TM
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INGREDIENTS AND APPEARANCE
CONTRAST ALLERGY PREMED PACK
prednisone, diphenhydramine kitProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:16129-101 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:16129-101-01 1 in 1 BLISTER PACK; Type 1: Convenience Kit of Co-Package 09/13/2016 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 3 Part 2 1 Part 1 of 2 PREDNISONE
prednisone tabletProduct Information Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PREDNISONE (UNII: VB0R961HZT) (PREDNISONE - UNII:VB0R961HZT) PREDNISONE 50 mg in 50 mg Product Characteristics Color white Score score with uneven pieces Shape ROUND Size 10mm Flavor Imprint Code Contains Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other Part 2 of 2 DIPHENHYDRAMINE HYDROCHLORIDE
diphenhydramine hydrochloride capsuleProduct Information Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE 50 mg in 50 mg Product Characteristics Color pink Score score with uneven pieces Shape CAPSULE Size 14mm Flavor Imprint Code Contains Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 09/13/2016 Labeler - Shertech Laboratories, LLC (621117279) Establishment Name Address ID/FEI Business Operations Shertech Laboratories, LLC 621117279 manufacture(16129-101)
