Acetaminophen and Codeine Phosphate

Product NDC
63629-2945
11-digit product format
636292945
Labeler code
63629
Product ID
63629-2945_36944332-572e-48f2-a230-9ec9fb7a219b
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Acetaminophen and Codeine Phosphate
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA088627
Marketing category
ANDA
Marketing start
1990-09-30
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
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
63629-2945-1EA - Each63629-2945e26dbd6c-c494-4a0c-bd2a-69ff6b5ba88812013-02-13