NDC 11822-6690

Acetaminophen Extended Release

Acetaminophen

Acetaminophen Extended Release is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Rite Aid Corporation. The primary component is Acetaminophen.

Product ID11822-6690_18ea1894-d6d7-4d24-b458-c47e93942f84
NDC11822-6690
Product TypeHuman Otc Drug
Proprietary NameAcetaminophen Extended Release
Generic NameAcetaminophen
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2019-08-12
Marketing CategoryANDA / ANDA
Application NumberANDA207035
Labeler NameRite Aid Corporation
Substance NameACETAMINOPHEN
Active Ingredient Strength650 mg/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 11822-6690-0

1 BOTTLE, PLASTIC in 1 BOX (11822-6690-0) > 50 TABLET in 1 BOTTLE, PLASTIC
Marketing Start Date2019-08-12
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 11822-6690-5 [11822669005]

Acetaminophen Extended Release TABLET
Marketing CategoryANDA
Application NumberANDA207035
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-08-12

NDC 11822-6690-1 [11822669001]

Acetaminophen Extended Release TABLET
Marketing CategoryANDA
Application NumberANDA207035
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-08-12

NDC 11822-6690-0 [11822669000]

Acetaminophen Extended Release TABLET
Marketing CategoryANDA
Application NumberANDA207035
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-08-12

Drug Details

Active Ingredients

IngredientStrength
ACETAMINOPHEN650 mg/1

OpenFDA Data

SPL SET ID:aa7c4bdd-ef58-485f-a9d6-99e0684851dc
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1148399
    • UPC Code
  • 0011822630276

    • NDC Crossover Matching brand name "Acetaminophen Extended Release" or generic name "Acetaminophen"

    NDCBrand NameGeneric Name
    0615-7590Acetaminophen Extended ReleaseAcetaminophen Extended Release
    11822-6690Acetaminophen Extended ReleaseAcetaminophen Extended Release
    41163-669Acetaminophen Extended ReleaseAcetaminophen Extended Release
    69842-093Acetaminophen Extended ReleaseAcetaminophen Extended Release
    11822-6304Acetaminophen Extended ReleaseAcetaminophen Extended Release
    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

    Trademark Results [Acetaminophen]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    ACETAMINOPHEN
    ACETAMINOPHEN
    85615223 not registered Dead/Abandoned
    General Merchandise importers and Expoters
    2012-05-03
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