Headache Relief

Product NDC
50844-334
11-digit product format
508440334
Labeler code
50844
Product ID
50844-334_35df517a-ca6d-4a2f-ab0d-5642318b9dcc
Type
HUMAN OTC DRUG
Nonproprietary name
Acetaminophen, Aspirin, Caffeine
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
L.N.K. International, Inc.
Application
part343
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2008-03-13
Marketing end
2023-08-10
Substance
ACETAMINOPHEN; ASPIRIN; CAFFEINE
Active strength
250 mg/1; mg/1; mg/1
Pharmacologic classes
Anti-Inflammatory Agents, Non-Steroidal [CS], Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE], Cyclooxygenase Inhibitors [MoA], Decreased Platelet Aggregation [PE], Decreased Prostaglandin Production [PE], Methylxanthine [EPC], Nonsteroidal Anti-inflammatory Drug [EPC], Platelet Aggregation Inhibitor [EPC], Xanthines [CS]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
50844-334-12508440334121 BOTTLE, PLASTIC in 1 CARTON (50844-334-12) > 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC2008-03-132023-08-10NoNoCurrent