NDC 58599-016

MEDPURINE

Medpurine

MEDPURINE is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Purinepharma Llc. The primary component is Aspirin.

• Product ID: 58599-016_eeab3524-4ac0-4ca7-9ac4-a6d2450971f6
• NDC: 58599-016
• Product Type: Human Otc Drug
• Proprietary Name: MEDPURINE
• Generic Name: Medpurine
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 2015-04-14
• Marketing Category: OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
• Application Number: part343
• Labeler Name: PURINEPHARMA LLC
• Substance Name: ASPIRIN
• Active Ingredient Strength: 81 mg/1
• NDC Exclude Flag: E
• Listing Certified Through: 2018-12-31

Packaging

NDC 58599-016-30

120 TABLET in 1 BOTTLE (58599-016-30)

• Marketing Start Date: 2015-04-14
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 58599-016-30 [58599001630]

MEDPURINE TABLET

• Marketing Category: OTC monograph final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2015-04-14
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
ASPIRIN	81 mg/1

OpenFDA Data

• SPL SET ID: 2b8a8124-9705-4335-b8bc-d36e37568333
• Manufacturer:
  • PURINEPHARMA LLC
• UNII:
  • R16CO5Y76E
• RxNorm Concept Unique ID - RxCUI:
  • 308416
• Pharm Class PE:
  • Decreased Prostaglandin Production [PE]
  • Decreased Platelet Aggregation [PE]
• PHarm Class EPC:
  • Nonsteroidal Anti-inflammatory Drug [EPC]
  • Platelet Aggregation Inhibitor [EPC]
• NUI Code:
  • N0000008832
  • N0000008836
  • N0000175721
  • N0000000160
  • N0000175578
  • N0000175722