NDC 33261-152

Adult Low Dose Aspirin

Aspirin

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

Product ID33261-152_896b0412-3ac7-470f-b96c-b3a6b50cf6a1
NDC33261-152
Product TypeHuman Otc Drug
Proprietary NameAdult Low Dose Aspirin
Generic NameAspirin
Dosage FormTablet, Delayed Release
Route of AdministrationORAL
Marketing Start Date2007-01-12
Marketing CategoryOTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
Application Numberpart343
Labeler NameAidarex Pharmaceuticals LLC
Substance NameASPIRIN
Active Ingredient Strength81 mg/1
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 33261-152-00

100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (33261-152-00)
Marketing Start Date2007-01-12
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 33261-152-90 [33261015290]

Adult Low Dose Aspirin TABLET, DELAYED RELEASE
Marketing CategoryOTC MONOGRAPH FINAL
Application Numberpart343
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2007-01-12
Inactivation Date2020-01-31

NDC 33261-152-09 [33261015209]

Adult Low Dose Aspirin TABLET, DELAYED RELEASE
Marketing CategoryOTC MONOGRAPH FINAL
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2007-01-12
Inactivation Date2020-01-31

NDC 33261-152-30 [33261015230]

Adult Low Dose Aspirin TABLET, DELAYED RELEASE
Marketing CategoryOTC MONOGRAPH FINAL
Application Numberpart343
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2007-01-12

NDC 33261-152-00 [33261015200]

Adult Low Dose Aspirin TABLET, DELAYED RELEASE
Marketing CategoryOTC MONOGRAPH FINAL
Application Numberpart343
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2007-01-12
Inactivation Date2020-01-31

NDC 33261-152-60 [33261015260]

Adult Low Dose Aspirin TABLET, DELAYED RELEASE
Marketing CategoryOTC MONOGRAPH FINAL
Application Numberpart343
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2007-01-12
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
ASPIRIN81 mg/1

OpenFDA Data

SPL SET ID:47b595dd-51ff-4400-91d5-c814a5c80eb4
Manufacturer
UNII
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

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

    NDCBrand NameGeneric Name
    0440-7135Adult Low Dose AspirinAdult Low Dose Aspirin
    16103-356Adult Low Dose AspirinAdult Low Dose Aspirin
    33261-152Adult Low Dose AspirinAdult Low Dose Aspirin
    50090-0552Adult Low Dose AspirinAdult Low Dose Aspirin
    72789-039Adult Low Dose AspirinAdult Low Dose Aspirin
    70934-495Adult Low Dose AspirinAdult Low Dose Aspirin
    0363-0157AspirinAspirin
    0363-0218AspirinAspirin
    0363-0227AspirinAspirin
    0113-0773Basic Care AspirinAspirin
    0113-7467basic care aspirinAspirin
    0280-2100BayerAspirin
    0280-2110Bayer Aspirin RegimenAspirin
    0280-2080Bayer Aspirin Regimen ChewableAspirin
    0280-2090Bayer Chewable - Aspirin RegimenAspirin
    0280-2000Bayer Genuine AspirinAspirin
    0280-2040Bayer PlusAspirin
    0280-2200Bayer WomensAspirin
    0067-6424BUFFERINASPIRIN
    0113-0259good sense aspirinAspirin
    0113-0274Good Sense aspirinAspirin
    0113-0416good sense aspirinAspirin
    0113-0467good sense aspirinAspirin
    0113-1919Good Sense Aspirinaspirin
    0363-0183Regular Strength Tri-Buffered AspirinAspirin
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