Donnatal - 17856-0423-5 - (phenobarbital elixir)

Alphabetical Index


Drug Information of Donnatal

Product NDC: 17856-0423
Proprietary Name: Donnatal
Non Proprietary Name: phenobarbital elixir
Active Ingredient(s): .0194; .1037; 16.2; .0065    mg/5mL; mg/5mL; mg/5mL; mg/5mL & nbsp;   phenobarbital elixir
Administration Route(s): ORAL
Dosage Form(s): ELIXIR
Coding System: National Drug Codes(NDC)

Labeler Information of Donnatal

Product NDC: 17856-0423
Labeler Name: Atlantic Biologicals Corps
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20091101

Package Information of Donnatal

Package NDC: 17856-0423-5
Package Description: 5 mL in 1 CUP (17856-0423-5)

NDC Information of Donnatal

NDC Code 17856-0423-5
Proprietary Name Donnatal
Package Description 5 mL in 1 CUP (17856-0423-5)
Product NDC 17856-0423
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name phenobarbital elixir
Dosage Form Name ELIXIR
Route Name ORAL
Start Marketing Date 20091101
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Atlantic Biologicals Corps
Substance Name ATROPINE SULFATE; HYOSCYAMINE SULFATE; PHENOBARBITAL; SCOPOLAMINE HYDROBROMIDE
Strength Number .0194; .1037; 16.2; .0065
Strength Unit mg/5mL; mg/5mL; mg/5mL; mg/5mL
Pharmaceutical Classes Anticholinergic [EPC],Cholinergic Antagonists [MoA],Anticholinergic [EPC],Cholinergic Antagonists [MoA],Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA]

Complete Information of Donnatal


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