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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 -
RANBAXY
New Drug Application (NDA) Number -
075132
Product Number -
001
Therapeutic Equivalence (TE) Code -
Approval Date -
Jan 14, 2000
Reference Listed Drug (RLD) -
No
Type -
OTC
Applicant Full Name -
Ranbaxy Laboratories Ltd
Ranitidine
Ranitidine Eq 300mg Base Tablet; Oral
Ranitidine Eq 75mg Base Tablet; 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Tablet, Effervescent; Oral Zantac 75 Eq 75mg Base **federal Register Determination That Product Was Not Discontinued Or Withdrawn For Safety Or Efficacy Reasons** Tablet, Effervescent; Oral Ranitidine Eq 75mg Base Tablet; Oral Ranitidine Eq 75mg Base Tablet; Oral Ranitidine Eq 75mg Base Tablet; Oral Ranitidine Eq 75mg Base Tablet; Oral Ranitidine Eq 75mg Base Tablet; Oral Ranitidine Eq 150mg Base Tablet; Oral NewDrugInformation |