ibuprofen pm

Product NDC
59779-413
11-digit product format
597790413
Labeler code
59779
Product ID
59779-413_885ee5e1-acc1-4b3d-9628-4d1d82c1ca33
Type
HUMAN OTC DRUG
Nonproprietary name
Diphenhydramine citrate, Ibuprofen
Dosage form
TABLET, COATED
Route
ORAL
Labeler
CVS Pharmacy
Application
ANDA079113
Marketing category
ANDA
Marketing start
2010-03-02
Marketing end
0000-00-00
Substance
DIPHENHYDRAMINE CITRATE; IBUPROFEN
Active strength
38 mg/1; mg/1
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
59779-413-27EA - Each59779-41366706eaf-373e-488b-9162-2ce44579e3c412022-06-06
59779-413-58EA - Each59779-413acadba2e-e014-4b97-b276-500dfee2f77812022-06-06
59779-413-60EA - Each59779-413b5f76670-fc49-4693-9f30-3727e1e7fa8612022-06-06