Metoprolol Tartrate

Product NDC
35356-889
11-digit product format
353560889
Labeler code
35356
Product ID
35356-889_a2561b14-d410-4e94-bf53-d61235ba7ead
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Metoprolol tartrate
Dosage form
TABLET
Route
ORAL
Labeler
Lake Erie Medical DBA Quality Care Products LLC
Application
ANDA074644
Marketing category
ANDA
Marketing start
1997-07-01
Marketing end
0000-00-00
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
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
35356-889-30EA - Each35356-889f4f8dc3a-d8f4-416a-b9d3-929232bebae612013-11-04
35356-889-60EA - Each35356-889c549ff4b-adb2-4c1e-a719-bd449eed07c412013-11-04
35356-889-90EA - Each35356-88993725eb0-4254-4657-974c-8b86cc5d0d2d12013-11-04