NDC 68788-9971

All Day Relief

Naproxen Sodium Tablet, Coated

All Day Relief is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Preferred Pharmaceuticals Inc.. The primary component is Naproxen Sodium.

Product ID68788-9971_37495b5f-dbb5-4163-b340-2b45fe4e6da6
NDC68788-9971
Product TypeHuman Otc Drug
Proprietary NameAll Day Relief
Generic NameNaproxen Sodium Tablet, Coated
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2015-05-06
Marketing CategoryANDA / ANDA
Application NumberANDA090545
Labeler NamePreferred Pharmaceuticals Inc.
Substance NameNAPROXEN SODIUM
Active Ingredient Strength220 mg/1
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 68788-9971-1

100 TABLET in 1 BOTTLE (68788-9971-1)
Marketing Start Date2015-05-06
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 68788-9971-6 [68788997106]

All Day Relief TABLET
Marketing CategoryANDA
Application NumberANDA090545
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-05-06
Marketing End Date2019-11-01

NDC 68788-9971-2 [68788997102]

All Day Relief TABLET
Marketing CategoryANDA
Application NumberANDA090545
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-05-06
Marketing End Date2019-11-01

NDC 68788-9971-3 [68788997103]

All Day Relief TABLET
Marketing CategoryANDA
Application NumberANDA090545
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-05-06
Marketing End Date2019-11-01

NDC 68788-9971-8 [68788997108]

All Day Relief TABLET
Marketing CategoryANDA
Application NumberANDA090545
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-05-06
Marketing End Date2019-11-01

NDC 68788-9971-4 [68788997104]

All Day Relief TABLET
Marketing CategoryANDA
Application NumberANDA090545
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-05-06
Marketing End Date2019-11-01

NDC 68788-9971-1 [68788997101]

All Day Relief TABLET
Marketing CategoryANDA
Application NumberANDA090545
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-05-06
Marketing End Date2019-11-01

NDC 68788-9971-9 [68788997109]

All Day Relief TABLET
Marketing CategoryANDA
Application NumberANDA090545
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-05-06
Marketing End Date2019-11-01

Drug Details

Active Ingredients

IngredientStrength
NAPROXEN SODIUM220 mg/1

OpenFDA Data

SPL SET ID:1812c18f-5472-4900-bb59-4e5bd80f3311
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 849574

    • NDC Crossover Matching brand name "All Day Relief" or generic name "Naproxen Sodium Tablet, Coated"

    NDCBrand NameGeneric Name
    0536-1022All Day ReliefNaproxen Sodium, Coated Tablets
    0536-1023All Day ReliefNaproxen Sodium Tablet, coated
    42507-140all day reliefNaproxen sodium
    42507-368all day reliefNaproxen Sodium
    52959-469all day reliefNaproxen Sodium
    56062-368All Day ReliefNaproxen Sodium
    56062-490all day reliefNaproxen Sodium
    56062-748All Day ReliefNaproxen Sodium
    68788-9971All Day ReliefNaproxen Sodium Tablet, coated
    25000-144Naproxen SodiumNaproxen Sodium Tablet, coated
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