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NANDROLONE

 
 
Content specific to this active ingredient…

Drug Information
Prescribing and patient information from leading authorities

Drug Master Files
Type 2 master files on file at the FDA

Safety Information
For prescription drugs containing this active ingredient

Exclusivity
Patent and market exclusivity data

Federal Register
FR search results for this API

FDA Approved Labelling
Information found in this drug's package inserts

Research Links
Chemical identification and research citations

Title 21 Code of Federal Regulations
FDA regulations for this API

 
 
 
 
 
 
 
 

 


 

FDA Approval Activities for this Drug…

NALIDIXIC ACID Tablet; 1GM NEGGRAM SANOFI SYNTHELABO | 014214 NALIDIXIC ACID Tablet; 250MG NEGGRAM SANOFI SYNTHELABO | 014214 NALIDIXIC ACID Tablet; 500MG NEGGRAM SANOFI SYNTHELABO | 071919 NALIDIXIC ACID Tablet; 1GM NALIDIXIC ACID Watson | 071936 NALIDIXIC ACID Tablet; 250MG NALIDIXIC ACID Watson 072061 NALIDIXIC ACID Tablet; 500MG NALIDIXIC ACID Watson | Nandrolone Decanoate Injection, PharmaForce, Inc., Approval

^ FDA's latest approval appears at the bottom of this list. ^

                                                                   

 

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