NDC 63868-144

Nasal Decongestant PE Non-Drowsy Maximum Strength

Phenylephrine Hcl

Nasal Decongestant PE Non-Drowsy Maximum Strength is a Oral Tablet, Film Coated in the Human Otc Drug category. It is labeled and distributed by Chain Drug Marketing Association Inc. The primary component is Phenylephrine Hydrochloride.

Product ID63868-144_0a5e1068-8b10-4acc-9b48-bed8a505f0bf
NDC63868-144
Product TypeHuman Otc Drug
Proprietary NameNasal Decongestant PE Non-Drowsy Maximum Strength
Generic NamePhenylephrine Hcl
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2005-01-14
Marketing CategoryOTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
Application Numberpart341
Labeler NameCHAIN DRUG MARKETING ASSOCIATION INC
Substance NamePHENYLEPHRINE HYDROCHLORIDE
Active Ingredient Strength10 mg/1
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 63868-144-19

1 BLISTER PACK in 1 CARTON (63868-144-19) > 18 TABLET, FILM COATED in 1 BLISTER PACK
Marketing Start Date2005-01-14
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 63868-144-19 [63868014419]

Nasal Decongestant PE Non-Drowsy Maximum Strength TABLET, FILM COATED
Marketing CategoryOTC MONOGRAPH FINAL
Application Numberpart341
Product TypeHUMAN OTC DRUG
Marketing Start Date2005-01-14

NDC 63868-144-74 [63868014474]

Nasal Decongestant PE Non-Drowsy Maximum Strength TABLET, FILM COATED
Marketing CategoryOTC MONOGRAPH FINAL
Application Numberpart341
Product TypeHUMAN OTC DRUG
Marketing Start Date2005-01-14
Marketing End Date2022-03-23

NDC 63868-144-23 [63868014423]

Nasal Decongestant PE Non-Drowsy Maximum Strength TABLET, FILM COATED
Marketing CategoryOTC MONOGRAPH FINAL
Application Numberpart341
Product TypeHUMAN OTC DRUG
Marketing Start Date2005-01-14
Marketing End Date2014-01-10

NDC 63868-144-37 [63868014437]

Nasal Decongestant PE Non-Drowsy Maximum Strength TABLET, FILM COATED
Marketing CategoryOTC MONOGRAPH FINAL
Application Numberpart341
Product TypeHUMAN OTC DRUG
Marketing Start Date2005-01-14

Drug Details

Active Ingredients

IngredientStrength
PHENYLEPHRINE HYDROCHLORIDE10 mg/1

OpenFDA Data

SPL SET ID:bf7246c1-90fe-4de8-8bb2-e5ff7e8ca63d
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1049182
  • UPC Code
  • 0635515955356
  • Medicade Reported Pricing

    63868014472 QC SUPHEDRINE PE 10 MG TABLET

    Pricing Unit: EA | Drug Type:

    63868014418 QC SUPHEDRINE PE 10 MG TABLET

    Pricing Unit: EA | Drug Type:

    NDC Crossover Matching brand name "Nasal Decongestant PE Non-Drowsy Maximum Strength" or generic name "Phenylephrine Hcl"

    NDCBrand NameGeneric Name
    63868-144Nasal Decongestant PE Non-Drowsy Maximum StrengthNasal Decongestant PE Non-Drowsy Maximum Strength
    0363-4531Nasal DecongestantPhenylephrine HCl
    30142-953Nasal DecongestantPhenylephrine HCl
    33992-0453Nasal DecongestantPhenylephrine HCl
    21130-453Nasal Decongestant PEPhenylephrine HCl
    37808-453Nasal Decongestant PEPhenylephrine HCl
    36800-704PE Sinus CongestionPhenylephrine HCl
    0536-1291Phenylephrine HClPhenylephrine HCl
    0924-0133PhysiciansCare SinusPhenylephrine HCL
    15127-081PSEUDO-FREE PEPhenylephrine HCl
    0031-9305Robitussin Direct Stuffy NosePhenylephrine hcl
    30142-853Sinus CongestionPhenylephrine HCl
    11673-453sinus PEPhenylephrine HCl
    11822-4530Sinus Pressure and Congestion Relief PEPhenylephrine HCl
    0904-5733Sudogest PEPhenylephrine HCl
    0363-0453Wal-Phed PEPhenylephrine HCl

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