NDC 68788-6408

Pharbetol

Acetaminophen

Pharbetol is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Preferred Pharmaceuticals, Inc.. The primary component is Acetaminophen.

Product ID68788-6408_72f92d38-97fc-4143-a87f-e514c4190d88
NDC68788-6408
Product TypeHuman Otc Drug
Proprietary NamePharbetol
Generic NameAcetaminophen
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2016-06-08
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart343
Labeler NamePreferred Pharmaceuticals, Inc.
Substance NameACETAMINOPHEN
Active Ingredient Strength500 mg/1
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 68788-6408-5

50 TABLET in 1 BOTTLE, PLASTIC (68788-6408-5)
Marketing Start Date2016-06-08
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 68788-6408-1 [68788640801]

Pharbetol TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-06-08
Inactivation Date2020-01-31

NDC 68788-6408-3 [68788640803]

Pharbetol TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-06-08
Inactivation Date2020-01-31

NDC 68788-6408-4 [68788640804]

Pharbetol TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-06-08
Inactivation Date2020-01-31

NDC 68788-6408-2 [68788640802]

Pharbetol TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-06-08
Inactivation Date2020-01-31

NDC 68788-6408-5 [68788640805]

Pharbetol TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-06-08
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
ACETAMINOPHEN500 mg/1

OpenFDA Data

SPL SET ID:ad3a5b2c-93e1-4d7d-94c9-636f5270dc0a
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 198440
  • 1293942

    • NDC Crossover Matching brand name "Pharbetol" or generic name "Acetaminophen"

    NDCBrand NameGeneric Name
    68788-6408PharbetolPharbetol
    16103-350PHARBETOLPHARBETOL
    16103-376PharbetolPharbetol
    50090-0395PharbetolPharbetol
    50090-1191PHARBETOLPHARBETOL
    73057-350PharbetolPharbetol
    73057-376PharbetolPharbetol
    73057-353PharbetolPharbetol
    61919-861PHARBETOLPHARBETOL
    71205-990PharbetolPharbetol
    71205-478PharbetolPharbetol
    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 [Pharbetol]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    PHARBETOL
    PHARBETOL
    78730584 3182003 Dead/Cancelled
    Pharbest Pharmaceuticals Inc.
    2005-10-11
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