NDC 65084-880

Acetaminophen 325mg RS

Acetaminophen 325mg

Acetaminophen 325mg RS is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Mckesson Corporation Dba Rx Pak. The primary component is Acetaminophen.

• Product ID: 65084-880_5b87d3be-2d15-4f6a-8ffd-afb6baa04aaf
• NDC: 65084-880
• Product Type: Human Otc Drug
• Proprietary Name: Acetaminophen 325mg RS
• Generic Name: Acetaminophen 325mg
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 2016-04-15
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part343
• Labeler Name: McKesson Corporation dba RX Pak
• Substance Name: ACETAMINOPHEN
• Active Ingredient Strength: 325 mg/1
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 65084-880-01

25 BLISTER PACK in 1 BOX (65084-880-01) > 30 TABLET in 1 BLISTER PACK

• Marketing Start Date: 2019-09-17
• Marketing End Date: 2021-07-31
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 65084-880-01 [65084088001]

Acetaminophen 325mg RS TABLET

• Marketing Category: OTC MONOGRAPH NOT FINAL
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2019-09-17

Drug Details

Active Ingredients

Ingredient	Strength
ACETAMINOPHEN	325 mg/1

OpenFDA Data

• SPL SET ID: 99702813-6071-4d47-9b22-a8d0fe0608c5
• Manufacturer:
  • McKesson Corporation dba RX Pak
• UNII:
  • 362O9ITL9D
• RxNorm Concept Unique ID - RxCUI:
  • 313782

NDC Crossover Matching brand name "Acetaminophen 325mg RS" or generic name "Acetaminophen 325mg"

NDC	Brand Name	Generic Name
72615-0001	Acetaminophen	Acetaminophen 325mg
63739-087	Acetaminophen 325mg	Acetaminophen 325mg
65084-880	Acetaminophen 325mg	Acetaminophen 325mg
69168-010	Acetaminophen 325mg	Acetaminophen 325mg
59961-141	Travel Savvy Non-Aspirin	Acetaminophen 325mg
59961-151	Travel Savvy Non-Aspirin	Acetaminophen 325mg