NDC Labeler Braintree Laboratories, Inc.

Braintree Laboratories, Inc. labeler's code is 52268. The labeler has 8 products that have an assigned National Drug Code.

NDC	Proprietary Name	Non-Proprietary Name	Dosage Form	Route Name	Product Type	Status
52268-012	Suprep Bowel Prep	Sodium Sulfate, Potassium Sulfate, Magnesium Sulfate	Solution, Concentrate	Oral	Human Prescription Drug	ACTIVE
52268-100	Golytely	Polyethylene Glycol 3350, Sodium Sulfate Anhydrous, Sodium Bicarbonate, Sodium Chloride, Potassium Chloride	Powder, For Solution	Oral	Human Prescription Drug	ACTIVE
52268-101	Golytely	Polyethylene Glycol 3350, Sodium Sulfate Anhydrous, Sodium Bicarbonate, Sodium Chloride, Potassium Chloride	Powder, For Solution	Oral	Human Prescription Drug	ACTIVE
52268-112	Suprep Bowel Prep	Sodium Sulfate, Potassium Sulfate, Magnesium Sulfate	Solution, Concentrate	Oral	Human Prescription Drug	ACTIVE
52268-201	Sutab	Sodium Sulfate, Magnesium Sulfate, And Potassium Chloride	Tablet	Oral	Human Prescription Drug	ACTIVE
52268-302	Nulytely	Polyethylene Glycol 3350, Sodium Chloride, Sodium Bicarbonate And Potassium Chloride	Powder, For Solution	Oral	Human Prescription Drug	ACTIVE
52268-400	Nulytely With Flavor Packs	Polyethylene Glycol 3350, Sodium Chloride, Sodium Bicarbonate And Potassium Chloride	Kit	Oral	Human Prescription Drug	ACTIVE
52268-600	Pizensy	Lactitol	Powder, For Solution	Oral	Human Prescription Drug	ACTIVE