equate all night pain relief

Product NDC
49035-727
11-digit product format
490350727
Labeler code
49035
Product ID
49035-727_4fe532c4-c665-4fd5-ab20-e4131029baf8
Type
HUMAN OTC DRUG
Nonproprietary name
diphenhydramine hydrochloride, naproxen sodium
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Wal-Mart Stores Inc
Application
ANDA208499
Marketing category
ANDA
Marketing start
2020-04-20
Marketing end
0000-00-00
Substance
DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM
Active strength
25 mg/1; mg/1
Pharmacologic classes
Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], Nonsteroidal Anti-inflammatory Drug [EPC]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49035-727EQUATE ALL NIGHT PAIN RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE, NAPROXEN SODIUM) TABLET, FILM COATED [WAL-MART STORES INC]4Legacy NDC20240907_2a766b70-e845-42bd-afb6-b4040ed334b0.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
49035-727-60490350727601 BOTTLE in 1 CARTON (49035-727-60) > 20 TABLET, FILM COATED in 1 BOTTLE1 bottle2020-04-200000-00-00NoNoCurrent