NDC 63868-146

Suphedrine Maximum Strength

Pseudoephedrine Hcl

Suphedrine 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 Pseudoephedrine Hydrochloride.

• Product ID: 63868-146_b359be70-3b20-492b-bfae-3f04b506bf99
• NDC: 63868-146
• Product Type: Human Otc Drug
• Proprietary Name: Suphedrine Maximum Strength
• Generic Name: Pseudoephedrine Hcl
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 1981-08-25
• Marketing End Date: 2020-02-22
• Marketing Category: OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
• Application Number: part341
• Labeler Name: CHAIN DRUG MARKETING ASSOCIATION INC
• Substance Name: PSEUDOEPHEDRINE HYDROCHLORIDE
• Active Ingredient Strength: 30 mg/1
• NDC Exclude Flag: N

Packaging

NDC 63868-146-48

2 BLISTER PACK in 1 CARTON (63868-146-48) > 24 TABLET, FILM COATED in 1 BLISTER PACK

• Marketing Start Date: 1981-08-25
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 63868-146-22 [63868014622]

Suphedrine Maximum Strength TABLET, FILM COATED

• Marketing Category: OTC MONOGRAPH FINAL
• Application Number: part341
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 1981-08-25
• Marketing End Date: 2016-11-22

NDC 63868-146-50 [63868014650]

Suphedrine Maximum Strength TABLET, FILM COATED

• Marketing Category: OTC MONOGRAPH FINAL
• Application Number: part341
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 1981-08-25
• Marketing End Date: 2016-11-22

NDC 63868-146-24 [63868014624]

Suphedrine Maximum Strength TABLET, FILM COATED

• Marketing Category: OTC MONOGRAPH FINAL
• Application Number: part341
• Product Type: HUMAN OTC DRUG
• Billing Unit: EA
• Marketing Start Date: 1981-08-25
• Marketing End Date: 2020-02-22

NDC 63868-146-48 [63868014648]

Suphedrine Maximum Strength TABLET, FILM COATED

• Marketing Category: OTC MONOGRAPH FINAL
• Application Number: part341
• Product Type: HUMAN OTC DRUG
• Billing Unit: EA
• Marketing Start Date: 1981-08-25
• Marketing End Date: 2020-02-22

Drug Details

Active Ingredients

Ingredient	Strength
PSEUDOEPHEDRINE HYDROCHLORIDE	30 mg/1

OpenFDA Data

• SPL SET ID: b407c167-1711-4455-8082-b56b22f5d379
• Manufacturer:
  • CHAIN DRUG MARKETING ASSOCIATION INC
• UNII:
  • 6V9V2RYJ8N
• RxNorm Concept Unique ID - RxCUI:
  • 1049160
• UPC Code:
  • 0635515945838

Medicade Reported Pricing

63868014648 QC SUPHEDRINE 30 MG TABLET

Pricing Unit: EA | Drug Type:

63868014624 SUPHEDRINE SINUS CONG 30 MG TB

Pricing Unit: EA | Drug Type:

NDC Crossover Matching brand name "Suphedrine Maximum Strength" or generic name "Pseudoephedrine Hcl"

NDC	Brand Name	Generic Name
63868-146	Suphedrine Maximum Strength	Suphedrine Maximum Strength
0113-0432	Good Sense Nasal Decongestant	Pseudoephedrine HCl
0113-2432	Nasal Decongestant	Pseudoephedrine HCl
0363-1214	Nasal Decongestant	Pseudoephedrine HCl
0536-3607	Nasal Decongestant	Pseudoephedrine HCl
0536-4391	Nasal Decongestant	Pseudoephedrine HCl
21130-112	Nasal Decongestant	Pseudoephedrine HCl
0904-6990	Pseudoephedrine HCl	Pseudoephedrine HCl
0113-2017	sinus 12 hour	Pseudoephedrine HCl
0113-2008	sinus congestion	Pseudoephedrine HCl
11822-0112	Sinus Pressure and Congestion Relief	Pseudoephedrine HCl
11822-0650	sinus pressure and congestion relief	Pseudoephedrine HCl
0904-5053	SudoGest	Pseudoephedrine HCl
0904-6338	SudoGest	PSEUDOEPHEDRINE HCL
0904-6754	SudoGest 12 Hour	Pseudoephedrine HCl
0904-6337	SudoGest Nasal Decongestant	Pseudoephedrine HCl
11673-112	up and up sinus 12 hour	Pseudoephedrine HCl
0363-0112	Wal-phed	Pseudoephedrine HCl
0363-0061	walphed d	Pseudoephedrine HCl