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 ID: 63868-144_0a5e1068-8b10-4acc-9b48-bed8a505f0bf
• NDC: 63868-144
• Product Type: Human Otc Drug
• Proprietary Name: Nasal Decongestant PE Non-Drowsy Maximum Strength
• Generic Name: Phenylephrine Hcl
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 2005-01-14
• Marketing Category: OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
• Application Number: part341
• Labeler Name: CHAIN DRUG MARKETING ASSOCIATION INC
• Substance Name: PHENYLEPHRINE HYDROCHLORIDE
• Active Ingredient Strength: 10 mg/1
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 63868-144-19

1 BLISTER PACK in 1 CARTON (63868-144-19) > 18 TABLET, FILM COATED in 1 BLISTER PACK

• Marketing Start Date: 2005-01-14
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 63868-144-19 [63868014419]

Nasal Decongestant PE Non-Drowsy Maximum Strength TABLET, FILM COATED

• Marketing Category: OTC MONOGRAPH FINAL
• Application Number: part341
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2005-01-14

NDC 63868-144-74 [63868014474]

Nasal Decongestant PE Non-Drowsy Maximum Strength TABLET, FILM COATED

• Marketing Category: OTC MONOGRAPH FINAL
• Application Number: part341
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2005-01-14
• Marketing End Date: 2022-03-23

NDC 63868-144-23 [63868014423]

Nasal Decongestant PE Non-Drowsy Maximum Strength TABLET, FILM COATED

• Marketing Category: OTC MONOGRAPH FINAL
• Application Number: part341
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2005-01-14
• Marketing End Date: 2014-01-10

NDC 63868-144-37 [63868014437]

Nasal Decongestant PE Non-Drowsy Maximum Strength TABLET, FILM COATED

• Marketing Category: OTC MONOGRAPH FINAL
• Application Number: part341
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2005-01-14

Drug Details

Active Ingredients

Ingredient	Strength
PHENYLEPHRINE HYDROCHLORIDE	10 mg/1

OpenFDA Data

• SPL SET ID: bf7246c1-90fe-4de8-8bb2-e5ff7e8ca63d
• Manufacturer:
  • CHAIN DRUG MARKETING ASSOCIATION INC
• UNII:
  • 04JA59TNSJ
• 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"

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