NDC 59726-256

All Day Pain Relief

Naproxen Sodium

All Day Pain Relief is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by P & L Development, Llc. The primary component is Naproxen Sodium.

Product ID59726-256_0b8db001-88e2-4096-9faa-09b0edb1083a
NDC59726-256
Product TypeHuman Otc Drug
Proprietary NameAll Day Pain Relief
Generic NameNaproxen Sodium
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2014-03-28
Marketing CategoryANDA / ANDA
Application NumberANDA091353
Labeler NameP & L Development, LLC
Substance NameNAPROXEN SODIUM
Active Ingredient Strength220 mg/1
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 59726-256-15

1 BOTTLE, PLASTIC in 1 BOX (59726-256-15) > 15 TABLET in 1 BOTTLE, PLASTIC
Marketing Start Date2014-03-28
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 59726-256-15 [59726025615]

All Day Pain Relief TABLET
Marketing CategoryANDA
Application NumberANDA091353
Product TypeHUMAN OTC DRUG
Marketing Start Date2014-03-28

Drug Details

Active Ingredients

IngredientStrength
NAPROXEN SODIUM220 mg/1

OpenFDA Data

SPL SET ID:43bfcaa2-1b0c-45c0-8a0b-80034d25ed00
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 849574
  • UPC Code
  • 0359726169158
  • 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

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