NDC 0363-0368

All Day Pain Relief

Naproxen Sodium

All Day Pain Relief is a Oral Tablet, Film Coated in the Human Otc Drug category. It is labeled and distributed by Walgreen Company. The primary component is Naproxen Sodium.

Product ID0363-0368_2292586d-ca11-4adf-ba33-dd01ec7de588
NDC0363-0368
Product TypeHuman Otc Drug
Proprietary NameAll Day Pain Relief
Generic NameNaproxen Sodium
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date1997-01-14
Marketing CategoryANDA / ANDA
Application NumberANDA074661
Labeler NameWalgreen Company
Substance NameNAPROXEN SODIUM
Active Ingredient Strength220 mg/1
Pharm ClassesAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 0363-0368-61

600 TABLET, FILM COATED in 1 BOTTLE (0363-0368-61)
Marketing Start Date2011-02-25
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0363-0368-76 [00363036876]

All Day Pain Relief TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA074661
Product TypeHUMAN OTC DRUG
Marketing Start Date2002-07-11

NDC 0363-0368-71 [00363036871]

All Day Pain Relief TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA074661
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date1997-01-14

NDC 0363-0368-52 [00363036852]

All Day Pain Relief TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA074661
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2009-01-21

NDC 0363-0368-37 [00363036837]

All Day Pain Relief TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA074661
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2014-07-31

NDC 0363-0368-79 [00363036879]

All Day Pain Relief TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA074661
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2010-02-19

NDC 0363-0368-61 [00363036861]

All Day Pain Relief TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA074661
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2011-02-25

NDC 0363-0368-82 [00363036882]

All Day Pain Relief TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA074661
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2000-05-26

NDC 0363-0368-62 [00363036862]

All Day Pain Relief TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA074661
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date1997-01-14

NDC 0363-0368-78 [00363036878]

All Day Pain Relief TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA074661
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date1997-01-14

Drug Details

Active Ingredients

IngredientStrength
NAPROXEN SODIUM220 mg/1

OpenFDA Data

SPL SET ID:318d4e2a-7108-4e88-8e56-5bec17ca4a3e
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 849574

    • NDC Crossover Matching brand name "All Day Pain Relief" or generic name "Naproxen Sodium"

    NDCBrand NameGeneric Name
    68210-0030ALL DAY PAIN RELIEFALL DAY PAIN RELIEF
    69517-109All Day Pain ReliefAll Day Pain Relief
    70005-008All Day Pain ReliefAll Day Pain Relief
    15127-168All Day Pain ReliefAll Day Pain Relief
    30142-168All Day Pain ReliefAll Day Pain Relief
    36800-256All Day Pain ReliefAll Day Pain Relief
    37808-259All Day Pain ReliefAll Day Pain Relief
    37205-744All Day Pain ReliefAll Day Pain Relief
    37808-068All Day Pain ReliefAll Day Pain Relief
    37808-339all day pain reliefall day pain relief
    37808-500All Day Pain ReliefAll Day Pain Relief
    41163-167All Day Pain ReliefAll Day Pain Relief
    41163-169All Day Pain ReliefAll Day Pain Relief
    42254-230all day pain reliefall day pain relief
    49781-145All Day Pain ReliefAll Day Pain Relief
    49781-101All Day Pain ReliefAll Day Pain Relief
    49781-046All Day Pain ReliefAll Day Pain Relief
    49781-146All Day Pain ReliefAll Day Pain Relief
    49781-047All Day Pain ReliefAll Day Pain Relief
    55315-168All Day Pain ReliefAll Day Pain Relief
    55315-256All Day Pain ReliefAll Day Pain Relief
    55315-255All Day Pain ReliefAll Day Pain Relief
    55315-169All Day Pain ReliefAll Day Pain Relief
    55319-417All Day Pain ReliefAll Day Pain Relief
    55319-604All Day Pain ReliefAll Day Pain Relief
    55319-174All Day Pain ReliefAll Day Pain Relief
    59726-169All Day Pain ReliefAll Day Pain Relief
    59779-172All Day Pain ReliefAll Day Pain Relief
    59726-023All Day Pain ReliefAll Day Pain Relief
    59726-168All Day Pain ReliefAll Day Pain Relief
    0363-0169All Day Pain ReliefAll Day Pain Relief
    59726-256All Day Pain ReliefAll Day Pain Relief
    0363-0168All Day Pain ReliefAll Day Pain Relief
    0363-0368All Day Pain ReliefAll Day Pain Relief
    0363-0938all day pain reliefall day pain relief
    63940-174All Day Pain ReliefAll Day Pain Relief
    0363-6099ALL DAY PAIN RELIEFALL DAY PAIN RELIEF
    0363-9608ALL DAY PAIN RELIEFALL DAY PAIN RELIEF
    0280-6000AleveNAPROXEN SODIUM
    0280-6010AleveNAPROXEN SODIUM
    0280-6020AleveNAPROXEN SODIUM
    0280-0041Aleve Headache PainNaproxen Sodium
    0113-7033basic care naproxen sodiumNaproxen Sodium
    0113-7368Basic Care Naproxen SodiumNaproxen Sodium
    0113-7901basic care naproxen sodiumNaproxen Sodium
    0113-0901Good Sense Naproxen SodiumNaproxen Sodium
    0113-1412good sense naproxen sodiumnaproxen sodium
    0113-1773good sense naproxen sodiumNaproxen Sodium
    0113-4368Good Sense Naproxen SodiumNaproxen Sodium
    0280-0270MenstridolNAPROXEN SODIUM
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