DONNATAL - 0179-0088-80 - (BELLADONNA ALKALOIDS W/ PHENOBARBITAL)

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Drug Information of DONNATAL

Product NDC: 0179-0088
Proprietary Name: DONNATAL
Non Proprietary Name: BELLADONNA ALKALOIDS W/ PHENOBARBITAL
Active Ingredient(s): .0194; .1037; 16.2; .0065    mg/5mL; mg/5mL; mg/5mL; mg/5mL & nbsp;   BELLADONNA ALKALOIDS W/ PHENOBARBITAL
Administration Route(s): ORAL
Dosage Form(s): ELIXIR
Coding System: National Drug Codes(NDC)

Labeler Information of DONNATAL

Product NDC: 0179-0088
Labeler Name: KAISER FOUNDATION HOSPITALS
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20110330

Package Information of DONNATAL

Package NDC: 0179-0088-80
Package Description: 10 mL in 1 CUP, UNIT-DOSE (0179-0088-80)

NDC Information of DONNATAL

NDC Code 0179-0088-80
Proprietary Name DONNATAL
Package Description 10 mL in 1 CUP, UNIT-DOSE (0179-0088-80)
Product NDC 0179-0088
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name BELLADONNA ALKALOIDS W/ PHENOBARBITAL
Dosage Form Name ELIXIR
Route Name ORAL
Start Marketing Date 20110330
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name KAISER FOUNDATION HOSPITALS
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],Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA],Anticholinergic [EPC],Cholinergic Antagonists [MoA]

Complete Information of DONNATAL


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