Acetaminophen and Codeine

Product NDC
50090-1574
11-digit product format
500901574
Labeler code
50090
Product ID
50090-1574_5382aa59-ba82-4e3b-88e4-f21d0d85a2ed
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Acetaminophen and Codeine
Dosage form
TABLET
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA040779
Marketing category
ANDA
Marketing start
2008-05-29
Marketing end
0000-00-00
Substance
ACETAMINOPHEN; CODEINE PHOSPHATE
Active strength
300 mg/1; mg/1
Pharmacologic classes
Full Opioid Agonists [MoA],Opioid Agonist [EPC]
DEA schedule
CIII
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50090-1574-0EA - Each50090-15749144cdc0-f28a-4c12-8579-6d001f6a585e12018-11-06