Visitor Monitoring Drug Details: ACETAMINOPHEN
 
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Drug Details

Drug Name: ACETAMINOPHEN
FDA Application No: (NDA) 018337
Active Ingredient(s): ACETAMINOPHEN
Company: ACTAVIS MID ATLANTIC
Original Approval or Tentative Approval Date: April 22, 1980
Chemical Type: 5 New manufacturer
Review Classification: S Standard review drug
 
Therapeutic Equivalents Labels are not available
Approval History, Letters, Reviews and Related Documents
 
You can see the products in the same application. The table can be sorted by clicking the header columns.
 
Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
ACETAMINOPHEN ACETAMINOPHEN650MGSUPPOSITORY; RECTAL OTC Yes None
ACETAMINOPHEN ACETAMINOPHEN325MGSUPPOSITORY; RECTAL OTC No None
ACETAMINOPHEN ACETAMINOPHEN120MGSUPPOSITORY; RECTAL OTC No None
INFANTS' FEVERALL ACETAMINOPHEN80MGSUPPOSITORY; RECTAL OTC No None


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