NuLYTELY is a Oral Powder, For Solution in the Human Prescription Drug category. It is labeled and distributed by Braintree Laboratories, Inc.. The primary component is Polyethylene Glycol 3350; Sodium Bicarbonate; Sodium Chloride; Potassium Chloride.
Product ID | 52268-302_a977fcc2-4904-feea-e053-2995a90a10f3 |
NDC | 52268-302 |
Product Type | Human Prescription Drug |
Proprietary Name | NuLYTELY |
Generic Name | Polyethylene Glycol 3350, Sodium Chloride, Sodium Bicarbonate And Potassium Chloride |
Dosage Form | Powder, For Solution |
Route of Administration | ORAL |
Marketing Start Date | 1991-04-22 |
Marketing Category | NDA / NDA |
Application Number | NDA019797 |
Labeler Name | Braintree Laboratories, Inc. |
Substance Name | POLYETHYLENE GLYCOL 3350; SODIUM BICARBONATE; SODIUM CHLORIDE; POTASSIUM CHLORIDE |
Active Ingredient Strength | 420 g/4L; g/4L; g/4L; g/4L |
Pharm Classes | Osmotic Activity [MoA],Osmotic Laxative [EPC],Stimulation Large Intestine Fluid/Electrolyte Secretion [PE],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA],Potassium Compounds [CS],Potassium Salt [EPC],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA] |
NDC Exclude Flag | N |
Listing Certified Through | 2021-12-31 |
Marketing Start Date | 1991-04-22 |
NDC Exclude Flag | N |
Sample Package? | N |
NDC | Brand Name | Generic Name |
---|---|---|
52268-302 | NuLYTELY | polyethylene glycol 3350, sodium chloride, sodium bicarbonate and potassium chloride |
52268-400 | NuLYTELY With Flavor Packs | Polyethylene Glycol 3350, sodium chloride, sodium bicarbonate and potassium chloride |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
NULYTELY 75047805 2020999 Live/Registered |
Braintree Laboratories, Inc. 1996-01-24 |
NULYTELY 73796743 1572848 Dead/Cancelled |
BRAINTREE LABORATORIES, INC. 1989-05-01 |