METOPROLOL TARTRATE

Product NDC
70518-4418
11-digit product format
705184418
Labeler code
70518
Product ID
70518-4418_3e8af959-432a-1981-e063-6294a90af048
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
METOPROLOL
Dosage form
TABLET
Route
ORAL
Labeler
REMEDYREPACK INC.
Application
ANDA202871
Marketing category
ANDA
Marketing start
2025-07-31
Substance
METOPROLOL TARTRATE
Active strength
50 mg/1
Pharmacologic classes
Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
W5S57Y3A5LMETOPROLOL TARTRATE56392-17-7METOPROLOL TARTRATE
GEB06NHM23METOPROLOL51384-51-1METOPROLOL

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
70518-4418-07051844180030 TABLET in 1 BLISTER PACK (70518-4418-0) 30 tablet2025-07-31NoNoHistorical
70518-4418-17051844180190 TABLET in 1 BOTTLE, PLASTIC (70518-4418-1) 90 tablet2025-08-25NoNoHistorical
70518-4418-27051844180230 TABLET in 1 BLISTER PACK (70518-4418-2) 30 tablet2025-09-11NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
METOPROLOL TARTRATEREMEDYREPACK INC.2025-09-11HUMAN PRESCRIPTION DRUG LABEL3