NDC 11673-306

up and up powderlax

Polyethylene Glycol 3350

up and up powderlax is a Oral Powder, For Solution in the Human Otc Drug category. It is labeled and distributed by Target Corporation. The primary component is Polyethylene Glycol 3350.

Product ID11673-306_2f92c1ca-982e-4427-a6ab-532a43fb9db6
NDC11673-306
Product TypeHuman Otc Drug
Proprietary Nameup and up powderlax
Generic NamePolyethylene Glycol 3350
Dosage FormPowder, For Solution
Route of AdministrationORAL
Marketing Start Date2009-10-07
Marketing CategoryANDA / ANDA
Application NumberANDA090685
Labeler NameTarget Corporation
Substance NamePOLYETHYLENE GLYCOL 3350
Active Ingredient Strength17 g/17g
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 11673-306-01

119 g in 1 BOTTLE (11673-306-01)
Marketing Start Date2019-04-12
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 11673-306-52 [11673030652]

up and up powderlax POWDER, FOR SOLUTION
Marketing CategoryANDA
Application NumberANDA090685
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2019-04-11

NDC 11673-306-09 [11673030609]

up and up powderlax POWDER, FOR SOLUTION
Marketing CategoryANDA
Application NumberANDA090685
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-10-21

NDC 11673-306-19 [11673030619]

up and up powderlax POWDER, FOR SOLUTION
Marketing CategoryANDA
Application NumberANDA090685
Product TypeHUMAN OTC DRUG
Marketing Start Date2013-10-09
Marketing End Date2016-02-03

NDC 11673-306-60 [11673030660]

up and up powderlax POWDER, FOR SOLUTION
Marketing CategoryANDA
Application NumberANDA090685
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-04-11

NDC 11673-306-03 [11673030603]

up and up powderlax POWDER, FOR SOLUTION
Marketing CategoryANDA
Application NumberANDA090685
Product TypeHUMAN OTC DRUG
Billing UnitGM
Marketing Start Date2009-10-07

NDC 11673-306-17 [11673030617]

up and up powderlax POWDER, FOR SOLUTION
Marketing CategoryANDA
Application NumberANDA090685
Product TypeHUMAN OTC DRUG
Marketing Start Date2014-08-27
Marketing End Date2016-10-28

NDC 11673-306-02 [11673030602]

up and up powderlax POWDER, FOR SOLUTION
Marketing CategoryANDA
Application NumberANDA090685
Product TypeHUMAN OTC DRUG
Billing UnitGM
Marketing Start Date2009-10-07

NDC 11673-306-01 [11673030601]

up and up powderlax POWDER, FOR SOLUTION
Marketing CategoryANDA
Application NumberANDA090685
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-04-12

NDC 11673-306-04 [11673030604]

up and up powderlax POWDER, FOR SOLUTION
Marketing CategoryANDA
Application NumberANDA090685
Product TypeHUMAN OTC DRUG
Marketing Start Date2014-03-03

Drug Details

Active Ingredients

IngredientStrength
POLYETHYLENE GLYCOL 335017 g/17g

OpenFDA Data

SPL SET ID:1bceb457-b24f-485d-bfe2-af4b7d38a5c2
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 876193
  • NDC Crossover Matching brand name "up and up powderlax" or generic name "Polyethylene Glycol 3350"

    NDCBrand NameGeneric Name
    11673-306up and up powderlaxup and up powderlax
    0113-7306Basic Care ClearlaxPolyethylene Glycol 3350
    0113-0306Good Sense Clear LaxPolyethylene Glycol 3350
    0113-1023good sense clearlaxPolyethylene Glycol 3350
    0113-6900injoy constipation reliefPolyethylene Glycol 3350
    0224-1890Mighty LaxPOLYETHYLENE GLYCOL 3350
    11523-4357MiraLAXPolyethylene Glycol 3350
    11523-7234MiraLAXPolyethylene Glycol 3350
    0904-6025peg 3350Polyethylene Glycol 3350
    0904-6422PEG 3350POLYETHYLENE GLYCOL 3350
    0574-0412Polyethylene Glycol 3350POLYETHYLENE GLYCOL 3350
    0722-6920Polyethylene Glycol 3350Polyethylene Glycol 3350
    0722-6921Polyethylene Glycol 3350Polyethylene Glycol 3350
    0904-6931Polyethylene glycol 3350Polyethylene glycol 3350
    10135-683Polyethylene Glycol 3350Polyethylene Glycol 3350
    0536-1052rugby PEG 3350POLYETHYLENE GLYCOL 3350
    0363-0306smooth laxPolyethylene Glycol 3350
    0363-0489Smooth LAXpolyethylene glycol 3350

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.