8 Hour Pain Relief

Product NDC
70677-1123
11-digit product format
706771123
Labeler code
70677
Product ID
70677-1123_fdb7c5a5-f0b1-deee-e053-6294a90a54bd
Type
HUMAN OTC DRUG
Nonproprietary name
Acetaminophen
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Labeler
STRATEGIC SOURCING SERVICES LLC
Application
ANDA211544
Marketing category
ANDA
Marketing start
2023-06-09
Substance
ACETAMINOPHEN
Active strength
650 mg/1
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
362O9ITL9DACETAMINOPHEN103-90-2ACETAMINOPHEN

Packages

Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
70677-1123-1706771123011 BOTTLE, PLASTIC in 1 CARTON (70677-1123-1) / 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC2023-06-09NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
1201A-FST-2023-0609STRATEGIC SOURCING SERVICES LLC2023-06-09HUMAN OTC DRUG LABEL2