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Belladonna and Opium - 0574-7045-12 - (ATROPA BELLADONNA and OPIUM)

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Drug Information of Belladonna and Opium

Product NDC: 0574-7045
Proprietary Name: Belladonna and Opium
Non Proprietary Name: ATROPA BELLADONNA and OPIUM
Active Ingredient(s): 16.2; 60    mg/1; mg/1 & nbsp;   ATROPA BELLADONNA and OPIUM
Administration Route(s): RECTAL
Dosage Form(s): SUPPOSITORY
Coding System: National Drug Codes(NDC)

Labeler Information of Belladonna and Opium

Product NDC: 0574-7045
Labeler Name: Paddock Laboratories, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 19940501

Package Information of Belladonna and Opium

Package NDC: 0574-7045-12
Package Description: 12 PACKET in 1 BOX (0574-7045-12) > 1 SUPPOSITORY in 1 PACKET

NDC Information of Belladonna and Opium

NDC Code 0574-7045-12
Proprietary Name Belladonna and Opium
Package Description 12 PACKET in 1 BOX (0574-7045-12) > 1 SUPPOSITORY in 1 PACKET
Product NDC 0574-7045
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ATROPA BELLADONNA and OPIUM
Dosage Form Name SUPPOSITORY
Route Name RECTAL
Start Marketing Date 19940501
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Paddock Laboratories, LLC
Substance Name ATROPA BELLADONNA; OPIUM
Strength Number 16.2; 60
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of Belladonna and Opium


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