Home NDC 37808-600 Aspirin 81 mg
Product NDC 37808-600
11-digit product format 378080600
Labeler code 37808
Product ID 37808-600_48c44192-8553-4973-ae8e-3175ce7655cb
Type HUMAN OTC DRUG
Nonproprietary name Aspirin
Dosage form TABLET, DELAYED RELEASE
Route ORAL
Labeler H E B
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2011-05-01
Substance ASPIRIN
Active strength 81 mg/1
Pharmacologic classes Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Decreased Platelet Aggregation [PE], Decreased Prostaglandin Production [PE], Nonsteroidal Anti-inflammatory Drug [EPC], Platelet Aggregation Inhibitor [EPC]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Aspirin 81 mg
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ASPIRIN 81 mg/1
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 37808-600-32 Aspirin 81 mg 1 in 1 CARTON TABLET, DELAYED RELEASE 1 17 37808-600-32 Aspirin 81 mg 120 in 1 BOTTLE, PLASTIC TABLET, DELAYED RELEASE 120 17
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded ASPIRIN ACTIVE INGREDIENT R16CO5Y76E ASPIRIN 81 MG (ASPIRIN) TABLET, COATED [H E B] 3 ASPIRIN ACTIVE MOIETY R16CO5Y76E ASPIRIN 81 MG (ASPIRIN) TABLET, COATED [H E B] 3 CELLULOSE, MICROCRYSTALLINE INACTIVE INGREDIENT OP1R32D61U ASPIRIN 81 MG (ASPIRIN) TABLET, COATED [H E B] 3 D&C YELLOW NO. 10 INACTIVE INGREDIENT 35SW5USQ3G ASPIRIN 81 MG (ASPIRIN) TABLET, COATED [H E B] 3 FD&C YELLOW NO. 6 INACTIVE INGREDIENT H77VEI93A8 ASPIRIN 81 MG (ASPIRIN) TABLET, COATED [H E B] 3 HYPROMELLOSES INACTIVE INGREDIENT 3NXW29V3WO ASPIRIN 81 MG (ASPIRIN) TABLET, COATED [H E B] 3 POLYDEXTROSE INACTIVE INGREDIENT VH2XOU12IE ASPIRIN 81 MG (ASPIRIN) TABLET, COATED [H E B] 3 POLYETHYLENE GLYCOLS INACTIVE INGREDIENT 3WJQ0SDW1A ASPIRIN 81 MG (ASPIRIN) TABLET, COATED [H E B] 3 SILICON DIOXIDE INACTIVE INGREDIENT ETJ7Z6XBU4 ASPIRIN 81 MG (ASPIRIN) TABLET, COATED [H E B] 3 SODIUM BICARBONATE INACTIVE INGREDIENT 8MDF5V39QO ASPIRIN 81 MG (ASPIRIN) TABLET, COATED [H E B] 3 TITANIUM DIOXIDE INACTIVE INGREDIENT 15FIX9V2JP ASPIRIN 81 MG (ASPIRIN) TABLET, COATED [H E B] 3 TRIACETIN INACTIVE INGREDIENT XHX3C3X673 ASPIRIN 81 MG (ASPIRIN) TABLET, COATED [H E B] 3 TRIETHYL CITRATE INACTIVE INGREDIENT 8Z96QXD6UM ASPIRIN 81 MG (ASPIRIN) TABLET, COATED [H E B] 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 37808-600 ASPIRIN 81 MG (ASPIRIN) TABLET, DELAYED RELEASE [H E B] 15 Current NDC, Legacy NDC, 2 package rows 20240925_72b16a5c-825f-4f3f-a8b3-b723e4242da7.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 78 of 79 · 1,579 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 37808-600-32 37808060032 1 BOTTLE, PLASTIC in 1 CARTON (37808-600-32) / 120 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC 2011-05-01 0000-00-00 No No Current