Oxycodone and Acetaminophen

Product NDC
63629-7748
11-digit product format
636297748
Labeler code
63629
Product ID
63629-7748_3cd81d92-7a23-41ec-ab28-ec15e84b2600
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Oxycodone and Acetaminophen
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA202677
Marketing category
ANDA
Marketing start
2012-01-17
Marketing end
0000-00-00
Substance
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Active strength
325 mg/1; mg/1
Pharmacologic classes
Full Opioid Agonists [MoA], Opioid Agonist [EPC]
DEA schedule
CII
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
63629-7748-3EA - Each63629-77482d7baf65-5097-42bf-88df-1e9da15fb20712020-07-13
63629-7748-5EA - Each63629-7748b7073a4e-e548-4cb2-9a73-5b2b6bf369e012019-02-13

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63629-7748-16362977480130 TABLET in 1 BOTTLE (63629-7748-1) 30 tablet2012-01-170000-00-00NoNoCurrent
63629-7748-263629774802120 TABLET in 1 BOTTLE (63629-7748-2) 120 tablet2012-01-170000-00-00NoNoCurrent
63629-7748-36362977480390 TABLET in 1 BOTTLE (63629-7748-3) 90 tablet2012-01-170000-00-00NoNoCurrent
63629-7748-46362977480428 TABLET in 1 BOTTLE (63629-7748-4) 28 tablet2012-01-170000-00-00NoNoCurrent
63629-7748-56362977480560 TABLET in 1 BOTTLE (63629-7748-5) 60 tablet2012-01-170000-00-00NoNoCurrent
63629-7748-66362977480620 TABLET in 1 BOTTLE (63629-7748-6) 20 tablet2012-01-170000-00-00NoNoCurrent
63629-7748-76362977480745 TABLET in 1 BOTTLE (63629-7748-7) 45 tablet2012-01-170000-00-00NoNoCurrent
63629-7748-86362977480875 TABLET in 1 BOTTLE (63629-7748-8) 75 tablet2012-01-170000-00-00NoNoCurrent
63629-7748-963629774809100 TABLET in 1 BOTTLE (63629-7748-9) 100 tablet2012-01-170000-00-00NoNoCurrent