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SucralfateDrug - Sucralfate The trade name of the product as shown on the labeling.
Dosage -
TABLET; ORAL
Active Ingredient(s) -
Sucralfate
Strength -
1GM
Applicant -
TEVA
New Drug Application (NDA) Number -
070848
Product Number -
001
Therapeutic Equivalence (TE) Code -
AB
Approval Date -
Mar 29, 1996
Reference Listed Drug (RLD) -
No
Type -
RX
Applicant Full Name -
Teva Pharmaceuticals Usa Inc
Sucralfate
Carafate 1gm Tablet; Oral
Sucralfate 1gm Tablet; Oral Sucralfate 1gm Tablet; Oral Quelicin Preservative Free 20mg/ml Injectable; Injection Quelicin Preservative Free 50mg/ml Injectable; Injection Succinylcholine Chloride 100mg/vial Injectable; Injection Succinylcholine Chloride 20mg/ml Injectable; Injection Sucostrin 100mg/ml Injectable; Injection Sucostrin 20mg/ml Injectable; Injection Carafate 1gm/10ml Suspension; Oral NewDrugInformation |