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Chromic ChlorideDrug - Chromic Chloride The trade name of the product as shown on the labeling.
Dosage -
INJECTABLE; INJECTION
Active Ingredient(s) -
Chromic Chloride
Strength -
EQ 0.004MG CHROMIUM/ML
Applicant -
AM PHARM PARTNERS
New Drug Application (NDA) Number -
019271
Product Number -
001
Therapeutic Equivalence (TE) Code -
Approval Date -
May 5, 1987
Reference Listed Drug (RLD) -
No
Type -
DISCN
Applicant Full Name -
American Pharmaceutical Partners Inc
Chromic Chloride
Ovidrel 0.25mg/vial Injectable; Injection
Ovidrel Eq 0.25mg /0.5ml Injectable; Subcutaneous Chromic Chloride Eq 0.004mg Chromium/ml Injectable; Injection Prevalite Eq 4gm Resin/scoopful Powder; Oral Questran Eq 4gm Resin/packet Powder; Oral Questran Eq 4gm Resin/scoopful Powder; Oral Questran Light Eq 4gm Resin/packet Powder; Oral Questran Light Eq 4gm Resin/scoopful Powder; Oral Questran Eq 1gm Resin Tablet; Oral Questran Eq 800mg Resin Tablet; Oral NewDrugInformation |