NDC 71309-103

Adult Low Dose

Aspirin 81 Mg

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

• Product ID: 71309-103_87401db3-7163-b48b-e053-2a95a90ac98f
• NDC: 71309-103
• Product Type: Human Otc Drug
• Proprietary Name: Adult Low Dose
• Generic Name: Aspirin 81 Mg
• Dosage Form: Tablet, Delayed Release
• Route of Administration: ORAL
• Marketing Start Date: 2016-02-09
• Marketing Category: OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
• Application Number: part343
• Labeler Name: Safrel Pharmaceuticals, LLC.
• Substance Name: ASPIRIN
• Active Ingredient Strength: 81 mg/1
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 71309-103-02

2 POUCH in 1 POUCH (71309-103-02) > 2 TABLET, DELAYED RELEASE in 1 POUCH

• Marketing Start Date: 2017-06-05
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 71309-103-50 [71309010350]

Adult Low Dose TABLET, DELAYED RELEASE

• Marketing Category: OTC monograph final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2017-06-05
• Marketing End Date: 2019-06-07

NDC 71309-103-60 [71309010360]

Adult Low Dose TABLET, DELAYED RELEASE

• Marketing Category: OTC monograph final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2017-06-05
• Marketing End Date: 2019-06-07

NDC 71309-103-65 [71309010365]

Adult Low Dose TABLET, DELAYED RELEASE

• Marketing Category: OTC monograph final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2016-02-09
• Marketing End Date: 2019-06-07

NDC 71309-103-30 [71309010330]

Adult Low Dose TABLET, DELAYED RELEASE

• Marketing Category: OTC monograph final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2016-02-09
• Marketing End Date: 2019-06-07

NDC 71309-103-02 [71309010302]

Adult Low Dose TABLET, DELAYED RELEASE

• Marketing Category: OTC monograph final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2017-06-05
• Marketing End Date: 2019-06-07

NDC 71309-103-01 [71309010301]

Adult Low Dose TABLET, DELAYED RELEASE

• Marketing Category: OTC monograph final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2017-06-05
• Marketing End Date: 2019-06-07

NDC 71309-103-25 [71309010325]

Adult Low Dose TABLET, DELAYED RELEASE

• Marketing Category: OTC monograph final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2017-06-05
• Marketing End Date: 2019-06-07

Drug Details

Active Ingredients

Ingredient	Strength
ASPIRIN	81 mg/1

OpenFDA Data

• SPL SET ID: 87401db3-7162-b48b-e053-2a95a90ac98f
• Manufacturer:
  • Safrel Pharmaceuticals, LLC.
• UNII:
  • R16CO5Y76E
• 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:
  • 0069517104601
• NUI Code:
  • N0000008832
  • N0000008836
  • N0000175721
  • N0000000160
  • N0000175578
  • N0000175722

NDC Crossover Matching brand name "Adult Low Dose" or generic name "Aspirin 81 Mg"

NDC	Brand Name	Generic Name
71309-003	Adult Low Dose	Aspirin 81 mg
71309-103	Adult Low Dose	Aspirin 81 mg
48433-129	Aspirin	Aspirin 81 mg
50090-2898	Aspirin	Aspirin 81 mg
63739-434	Aspirin	Aspirin 81 mg
69168-288	Aspirin	Aspirin 81 mg
69168-318	ASPIRIN	Aspirin 81 MG
69168-372	Aspirin	Aspirin 81 mg
71872-7087	Aspirin	Aspirin 81 mg
69517-104	Pain Reliever	Aspirin 81 mg
71679-104	Pain Reliever	Aspirin 81 mg