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Cholestyramine LightDrug - Cholestyramine Light The trade name of the product as shown on the labeling.
Dosage -
POWDER; ORAL
Active Ingredient(s) -
Cholestyramine
Strength -
EQ 4GM RESIN/PACKET
Applicant -
PAR PHARM
New Drug Application (NDA) Number -
077203
Product Number -
001
Therapeutic Equivalence (TE) Code -
AB
Approval Date -
Aug 26, 2005
Reference Listed Drug (RLD) -
No
Type -
RX
Applicant Full Name -
Par Pharmaceutical Inc
Cholestyramine Light
Cholestyramine Light Eq 4gm Resin/packet Powder; Oral
Cholestyramine Eq 4gm Resin/scoopful Powder; Oral Cholestyramine Eq 4gm Resin/packet Powder; Oral Cholestyramine Eq 4gm Resin/scoopful Powder; Oral Cholestyramine Eq 4gm Resin/packet Powder; Oral Cholestyramine Eq 4gm Resin/scoopful Powder; Oral Cholestyramine Eq 4gm Resin/packet Powder; Oral Cholestyramine Eq 4gm Resin/scoopful Powder; Oral Cholestyramine Eq 4gm Resin/packet Powder; Oral Cholestyramine Eq 4gm Resin/scoopful Powder; Oral NewDrugInformation |