NDC 50332-0127

Relief-PE

Acetaminophen, Phenylephrine, Chlorpheniramine

Relief-PE is a Oral Tablet, Coated in the Human Otc Drug category. It is labeled and distributed by Normed. The primary component is Acetaminophen; Phenylephrine Hydrochloride; Chlorpheniramine Maleate.

• Product ID: 50332-0127_cdc37028-7070-4541-8d4a-52507e512a6b
• NDC: 50332-0127
• Product Type: Human Otc Drug
• Proprietary Name: Relief-PE
• Generic Name: Acetaminophen, Phenylephrine, Chlorpheniramine
• Dosage Form: Tablet, Coated
• Route of Administration: ORAL
• Marketing Start Date: 2012-04-16
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part343
• Labeler Name: NorMed
• Substance Name: ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE; CHLORPHENIRAMINE MALEATE
• Active Ingredient Strength: 325 mg/1; mg/1; mg/1
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 50332-0127-7

250 TABLET, COATED in 1 BOX, UNIT-DOSE (50332-0127-7)

• Marketing Start Date: 2012-04-16
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 50332-0127-7 [50332012707]

Relief-PE TABLET, COATED

• Marketing Category: OTC monograph not final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2012-04-16
• Inactivation Date: 2019-11-13

NDC 50332-0127-4 [50332012704]

Relief-PE TABLET, COATED

• Marketing Category: OTC monograph not final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2012-04-16
• Inactivation Date: 2019-11-13

Drug Details

Active Ingredients

Ingredient	Strength
ACETAMINOPHEN	325 mg/1

OpenFDA Data

• SPL SET ID: 96dcd0ed-9747-4e76-8d59-990b36acd8ec
• Manufacturer:
  • NorMed
• UNII:
  • V1Q0O9OJ9Z
  • 362O9ITL9D
  • 04JA59TNSJ
• RxNorm Concept Unique ID - RxCUI:
  • 1046781