NDC 11822-0519

pain relief acetaminophen Extra Strength

Acetaminophen

pain relief acetaminophen Extra Strength is a Oral Tablet, Coated in the Human Otc Drug category. It is labeled and distributed by Rite Aid Corporation. The primary component is Acetaminophen.

Product ID11822-0519_145f165b-4c93-4fd9-a28a-ae883a1733e1
NDC11822-0519
Product TypeHuman Otc Drug
Proprietary Namepain relief acetaminophen Extra Strength
Generic NameAcetaminophen
Dosage FormTablet, Coated
Route of AdministrationORAL
Marketing Start Date2004-05-10
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart343
Labeler NameRite Aid Corporation
Substance NameACETAMINOPHEN
Active Ingredient Strength500 mg/1
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 11822-0519-1

1 BLISTER PACK in 1 CARTON (11822-0519-1) > 2 TABLET, COATED in 1 BLISTER PACK
Marketing Start Date2004-05-10
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 11822-0519-9 [11822051909]

pain relief acetaminophen Extra Strength TABLET
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2004-05-10

NDC 11822-0519-1 [11822051901]

pain relief acetaminophen Extra Strength TABLET
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2004-05-10

NDC 11822-0519-2 [11822051902]

pain relief acetaminophen Extra Strength TABLET
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2004-05-10

NDC 11822-0519-5 [11822051905]

pain relief acetaminophen Extra Strength TABLET
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2004-05-10

NDC 11822-0519-3 [11822051903]

pain relief acetaminophen Extra Strength TABLET
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2004-05-10

NDC 11822-0519-4 [11822051904]

pain relief acetaminophen Extra Strength TABLET
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2004-05-10
Marketing End Date2015-01-05

Drug Details

Active Ingredients

IngredientStrength
ACETAMINOPHEN500 mg/1

OpenFDA Data

SPL SET ID:26c0641e-1cdd-4084-939d-01dbd36ab9b7
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 198440
  • NDC Crossover Matching brand name "pain relief acetaminophen Extra Strength" or generic name "Acetaminophen"

    NDCBrand NameGeneric Name
    11822-0519pain relief acetaminophen Extra Strengthpain relief acetaminophen Extra Strength
    0121-0657AcetaminophenAcetaminophen
    0113-7000Basic Care acetaminophenAcetaminophen
    0113-7484basic care acetaminophenAcetaminophen
    0113-7544Basic Care AcetaminophenAcetaminophen
    0113-7130basic care childrens pain and feverAcetaminophen
    0113-0020good sense childrens pain and feverAcetaminophen
    0113-0212Good Sense Childrens Pain and FeverAcetaminophen
    0113-0608good sense childrens pain and feverAcetaminophen
    0113-0998Good Sense Childrens Pain and FeverAcetaminophen
    0113-0161Good Sense pain and feverAcetaminophen
    0113-0397Good Sense Pain and Feveracetaminophen
    0113-0590Good Sense Pain and Feveracetaminophen
    0113-0946good sense pain and feverAcetaminophen
    0113-8959Good Sense Pain and FeverAcetaminophen
    0113-0025Good Sense Pain ReliefAcetaminophen
    0113-0044Good Sense Pain ReliefAcetaminophen
    0113-0187good sense pain reliefAcetaminophen
    0113-0217good sense pain reliefAcetaminophen
    0113-0227Good Sense Pain ReliefAcetaminophen
    0113-0403good sense pain reliefAcetaminophen
    0113-0484Good Sense Pain ReliefAcetaminophen
    0113-0518good sense pain reliefAcetaminophen
    0113-0544good sense pain reliefAcetaminophen
    0113-1889good sense pain reliefacetaminophen
    0113-1975Good Sense Pain ReliefAcetaminophen
    0031-9301Robitussin Direct Sore Throat Painacetaminophen

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