|
RanitidineDrug - Ranitidine The trade name of the product as shown on the labeling.
Dosage -
TABLET; ORAL
Active Ingredient(s) -
Ranitidine Hydrochloride
Strength -
EQ 75MG BASE
Applicant -
DR REDDYS LABS LTD
New Drug Application (NDA) Number -
075294
Product Number -
001
Therapeutic Equivalence (TE) Code -
Approval Date -
Mar 28, 2000
Reference Listed Drug (RLD) -
No
Type -
OTC
Applicant Full Name -
Dr Reddys Laboratories Ltd
Ranitidine
Zantac Eq 15mg Base/ml Syrup; Oral
Zantac 150 Eq 150mg Base Tablet, Effervescent; Oral Zantac 25 Eq 25mg Base Tablet, Effervescent; Oral Zantac 75 Eq 75mg Base **federal Register Determination That Product Was Not Discontinued Or Withdrawn For Safety Or Efficacy Reasons** Tablet, Effervescent; Oral Ranitidine Eq 75mg Base Tablet; Oral Ranitidine Eq 25mg Base/ml Injectable; Injection Ranitidine Hcl Eq 25mg Base/ml Injectable; Injection Zantac Eq 25mg Base/ml Injectable; Injection Zantac In Plastic Container Eq 1mg Base/ml Injectable; Injection Zantac In Plastic Container Eq 50mg Base/100ml Injectable; Injection NewDrugInformation |