NDC 63029-301

Ecotrin

Aspirin

Ecotrin is a Oral Tablet, Coated in the Human Otc Drug category. It is labeled and distributed by Medtech Products Inc.. The primary component is Aspirin.

• Product ID: 63029-301_ae512c15-44c0-4c87-8fee-1d144546e121
• NDC: 63029-301
• Product Type: Human Otc Drug
• Proprietary Name: Ecotrin
• Generic Name: Aspirin
• Dosage Form: Tablet, Coated
• Route of Administration: ORAL
• Marketing Start Date: 2012-06-01
• Marketing Category: OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
• Application Number: part343
• Labeler Name: Medtech Products Inc.
• Substance Name: ASPIRIN
• Active Ingredient Strength: 81 mg/1
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 63029-301-65

365 TABLET, COATED in 1 BOTTLE, PLASTIC (63029-301-65)

• Marketing Start Date: 2012-06-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 63029-301-65 [63029030165]

Ecotrin TABLET, COATED

• Marketing Category: OTC MONOGRAPH FINAL
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2012-07-16
• Inactivation Date: 2019-11-13

NDC 63029-301-45 [63029030145]

Ecotrin TABLET, COATED

• Marketing Category: OTC MONOGRAPH FINAL
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2012-07-16
• Inactivation Date: 2019-11-13

NDC 63029-301-08 [63029030108]

Ecotrin TABLET, COATED

• Marketing Category: OTC MONOGRAPH FINAL
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2012-07-16
• Inactivation Date: 2019-11-13

NDC 63029-301-01 [63029030101]

Ecotrin TABLET, COATED

• Marketing Category: OTC MONOGRAPH FINAL
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2012-06-01
• Inactivation Date: 2019-11-13

NDC 63029-301-07 [63029030107]

Ecotrin TABLET, COATED

• Marketing Category: OTC MONOGRAPH FINAL
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2012-07-16
• Inactivation Date: 2019-11-13

NDC 63029-301-14 [63029030114]

Ecotrin TABLET, COATED

• Marketing Category: OTC MONOGRAPH FINAL
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2012-07-16
• Inactivation Date: 2019-11-13

Drug Details

Active Ingredients

Ingredient	Strength
ASPIRIN	81 mg/1

OpenFDA Data

• SPL SET ID: f950d4eb-39b9-4ef7-b5f3-0cf45d4d6bc0
• Manufacturer:
  • Medtech Products Inc.
• UNII:
  • R16CO5Y76E
• RxNorm Concept Unique ID - RxCUI:
  • 1189781
  • 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

NDC Crossover Matching brand name "Ecotrin" or generic name "Aspirin"

NDC	Brand Name	Generic Name
63029-301	Ecotrin	Ecotrin
63029-311	Ecotrin	Ecotrin
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