NDC 10237-907

Legatrin PM

Acetaminophen, Diphenhydramine Hci

Legatrin PM is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Church & Dwight Co., Inc.. The primary component is Acetaminophen; Diphenhydramine Hydrochloride.

• Product ID: 10237-907_2dcf1c25-6dcb-4891-87f8-f33908d7357f
• NDC: 10237-907
• Product Type: Human Otc Drug
• Proprietary Name: Legatrin PM
• Generic Name: Acetaminophen, Diphenhydramine Hci
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 2014-10-01
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part343
• Labeler Name: Church & Dwight Co., Inc.
• Substance Name: ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE
• Active Ingredient Strength: 500 1/1; 1/1
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 10237-907-50

1 BOTTLE in 1 CARTON (10237-907-50) > 50 TABLET in 1 BOTTLE

• Marketing Start Date: 2014-10-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 10237-907-50 [10237090750]

Legatrin PM TABLET

• Marketing Category: OTC monograph not final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2014-10-01

Drug Details

Active Ingredients

Ingredient	Strength
ACETAMINOPHEN	500 1/1

OpenFDA Data

• SPL SET ID: 058be7e6-01cb-5cd6-e054-00144ff88e88
• Manufacturer:
  • Church & Dwight Co., Inc.
• UNII:
  • TC2D6JAD40
  • 362O9ITL9D
• RxNorm Concept Unique ID - RxCUI:
  • 1087607
  • 1087609