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Last Updated: November 22, 2024

Details for New Drug Application (NDA): 206105


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NDA 206105 describes POLYETHYLENE GLYCOL 3350, which is a drug marketed by Ani Pharms, Annora Pharma, Aurobindo Pharma Ltd, Breckenridge Pharm, Elysium, Lgm Pharma, Mylan, Nexgen Pharma Inc, Novel Labs Inc, Nuvo Pharms Inc, Paddock Llc, Ppi-dac, Strides Pharma, and Teva Pharms, and is included in eighteen NDAs. It is available from sixty-three suppliers. Additional details are available on the POLYETHYLENE GLYCOL 3350 profile page.

The generic ingredient in POLYETHYLENE GLYCOL 3350 is polyethylene glycol 3350; potassium chloride; sodium bicarbonate; sodium chloride; sodium sulfate anhydrous. There are four hundred and twenty-one drug master file entries for this compound. Six suppliers are listed for this compound. Additional details are available on the polyethylene glycol 3350; potassium chloride; sodium bicarbonate; sodium chloride; sodium sulfate anhydrous profile page.
Summary for 206105
Tradename:POLYETHYLENE GLYCOL 3350
Applicant:Nuvo Pharms Inc
Ingredient:polyethylene glycol 3350
Patents:0
Pharmacology for NDA: 206105
Suppliers and Packaging for NDA: 206105
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
POLYETHYLENE GLYCOL 3350 polyethylene glycol 3350 FOR SOLUTION;ORAL 206105 ANDA SUNRISE PHARMACEUTICAL, INC 11534-180 11534-180-19 119 g in 1 BOTTLE (11534-180-19)
POLYETHYLENE GLYCOL 3350 polyethylene glycol 3350 FOR SOLUTION;ORAL 206105 ANDA SUNRISE PHARMACEUTICAL, INC 11534-180 11534-180-28 238 g in 1 BOTTLE (11534-180-28)

Profile for product number 001

Active Rx/OTC/Discontinued:OTCDosage:FOR SOLUTION;ORALStrength17GM/SCOOPFUL
Approval Date:Oct 28, 2016TE:RLD:No

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