NDC 41250-780

Aspirin 81 mg

Aspirin

Aspirin 81 mg is a Oral Tablet, Delayed Release in the Human Otc Drug category. It is labeled and distributed by Meijer. The primary component is Aspirin.

• Product ID: 41250-780_34da761f-528b-2f20-e054-00144ff88e88
• NDC: 41250-780
• Product Type: Human Otc Drug
• Proprietary Name: Aspirin 81 mg
• Generic Name: Aspirin
• Dosage Form: Tablet, Delayed Release
• Route of Administration: ORAL
• Marketing Start Date: 2011-04-01
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part343
• Labeler Name: Meijer
• Substance Name: ASPIRIN
• Active Ingredient Strength: 81 mg/1
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 41250-780-01

1 BOTTLE, PLASTIC in 1 PACKAGE (41250-780-01) > 120 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC

• Marketing Start Date: 2011-03-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 41250-780-08 [41250078008]

Aspirin 81 MG TABLET, DELAYED RELEASE

• Marketing Category: OTC monograph not final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2011-04-01
• Marketing End Date: 2019-09-03

NDC 41250-780-14 [41250078014]

Aspirin 81 MG TABLET, DELAYED RELEASE

• Marketing Category: OTC monograph not final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2018-07-01

NDC 41250-780-01 [41250078001]

Aspirin 81 MG TABLET, DELAYED RELEASE

• Marketing Category: OTC monograph not final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2011-03-01

NDC 41250-780-06 [41250078006]

Aspirin 81 MG TABLET, DELAYED RELEASE

• Marketing Category: OTC monograph not final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2017-12-01

NDC 41250-780-12 [41250078012]

Aspirin 81 MG TABLET, DELAYED RELEASE

• Marketing Category: OTC monograph not final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2014-12-01

Drug Details

Active Ingredients

Ingredient	Strength
ASPIRIN	81 mg/1

OpenFDA Data

• SPL SET ID: b3e5711c-9529-4eec-871d-de8efa858b86
• Manufacturer:
  • Meijer
• 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]
• UPC Code:
  • 0708820876903
• NUI Code:
  • N0000008832
  • N0000008836
  • N0000175721
  • N0000000160
  • N0000175578
  • N0000175722

NDC Crossover Matching brand name "Aspirin 81 mg" or generic name "Aspirin"

NDC	Brand Name	Generic Name
69618-014	Aspirin 81 mg	Aspirin 81 mg
37808-600	Aspirin 81 mg	Aspirin 81 mg
41250-780	Aspirin 81 mg	Aspirin 81 mg
55910-600	Aspirin 81 mg	Aspirin 81 mg
63868-373	Aspirin 81 mg	Aspirin 81 mg
70297-018	Aspirin 81 mg	Aspirin 81 mg
71679-010	Aspirin 81 mg	Aspirin 81 mg
72629-020	Aspirin 81 mg	Aspirin 81 mg
0363-0157	Aspirin	Aspirin
0363-0218	Aspirin	Aspirin
0363-0227	Aspirin	Aspirin
0113-0773	Basic Care Aspirin	Aspirin
0113-7467	basic care aspirin	Aspirin
0280-2100	Bayer	Aspirin
0280-2110	Bayer Aspirin Regimen	Aspirin
0280-2080	Bayer Aspirin Regimen Chewable	Aspirin
0280-2090	Bayer Chewable - Aspirin Regimen	Aspirin
0280-2000	Bayer Genuine Aspirin	Aspirin
0280-2040	Bayer Plus	Aspirin
0280-2200	Bayer Womens	Aspirin
0067-6424	BUFFERIN	ASPIRIN
0113-0259	good sense aspirin	Aspirin
0113-0274	Good Sense aspirin	Aspirin
0113-0416	good sense aspirin	Aspirin
0113-0467	good sense aspirin	Aspirin
0113-1919	Good Sense Aspirin	aspirin
0363-0183	Regular Strength Tri-Buffered Aspirin	Aspirin