Sunmark Pain Reliever

Product NDC
49348-730
11-digit product format
493480730
Labeler code
49348
Product ID
49348-730_0401dedc-0400-4af6-91c3-485ba8ee3e2c
Type
HUMAN OTC DRUG
Nonproprietary name
Acetaminophen
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Strategic Sourcing Services LLC
Application
part343
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2005-12-27
Marketing end
0000-00-00
Substance
ACETAMINOPHEN
Active strength
500 mg/1
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
49348-730-09EA - Each49348-73088b583f5-8c67-40f3-9cbd-4fb4512c514e12012-07-24
49348-730-10EA - Each49348-7308635adbc-9fa2-4752-83dd-a5800c78a1e512012-07-24

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
49348-730-09493480730091 BOTTLE in 1 CARTON (49348-730-09) > 50 TABLET, FILM COATED in 1 BOTTLE1 bottle2005-12-270000-00-00NoNoCurrent
49348-730-10493480730101 BOTTLE in 1 CARTON (49348-730-10) > 100 TABLET, FILM COATED in 1 BOTTLE1 bottle2005-12-270000-00-00NoNoCurrent