NDC 75942-001

Adult Low Dose Aspirin Enteric Safety Coated

Aspirin

Adult Low Dose Aspirin Enteric Safety Coated is a Oral Tablet, Delayed Release in the Human Otc Drug category. It is labeled and distributed by Zandi Llc. The primary component is Aspirin.

• Product ID: 75942-001_c0e15e03-c564-428a-b6c9-46d114062fd2
• NDC: 75942-001
• Product Type: Human Otc Drug
• Proprietary Name: Adult Low Dose Aspirin Enteric Safety Coated
• Generic Name: Aspirin
• Dosage Form: Tablet, Delayed Release
• Route of Administration: ORAL
• Marketing Start Date: 2011-01-18
• Marketing Category: OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
• Application Number: part343
• Labeler Name: Zandi LLC
• Substance Name: ASPIRIN
• Active Ingredient Strength: 81 mg/1
• NDC Exclude Flag: E
• Listing Certified Through: 2018-12-31

Packaging

NDC 75942-001-12

120 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (75942-001-12)

• Marketing Start Date: 2011-01-18
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 75942-001-75 [75942000175]

Adult Low Dose Aspirin Enteric Safety Coated TABLET, DELAYED RELEASE

• Marketing Category: OTC monograph final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2011-01-18
• Inactivation Date: 2020-01-31

NDC 75942-001-36 [75942000136]

Adult Low Dose Aspirin Enteric Safety Coated TABLET, DELAYED RELEASE

• Marketing Category: OTC monograph final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2011-01-18
• Inactivation Date: 2020-01-31

NDC 75942-001-50 [75942000150]

Adult Low Dose Aspirin Enteric Safety Coated TABLET, DELAYED RELEASE

• Marketing Category: OTC monograph final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2011-01-18
• Inactivation Date: 2020-01-31

NDC 75942-001-12 [75942000112]

Adult Low Dose Aspirin Enteric Safety Coated TABLET, DELAYED RELEASE

• Marketing Category: OTC monograph final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2011-01-18
• Inactivation Date: 2020-01-31

NDC 75942-001-10 [75942000110]

Adult Low Dose Aspirin Enteric Safety Coated TABLET, DELAYED RELEASE

• Marketing Category: OTC monograph final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2011-01-18
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
ASPIRIN	81 mg/1

OpenFDA Data

• SPL SET ID: a03d1d10-1aa3-40cf-97f3-16c86596e9c3
• Manufacturer:
  • Zandi 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]
• UPC Code:
  • 0013964101607
• NUI Code:
  • N0000008832
  • N0000008836
  • N0000175721
  • N0000000160
  • N0000175578
  • N0000175722

NDC Crossover Matching brand name "Adult Low Dose Aspirin Enteric Safety Coated" or generic name "Aspirin"

NDC	Brand Name	Generic Name
75942-001	Adult Low Dose Aspirin Enteric Safety Coated	Adult Low Dose Aspirin Enteric Safety Coated
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