Metoprolol Tartrate

Product NDC
68788-6907
11-digit product format
687886907
Labeler code
68788
Product ID
68788-6907_b5660417-bb0d-483e-af27-2407ec184304
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Metoprolol Tartrate
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Preferred Pharmaceuticals Inc.
Application
ANDA077739
Marketing category
ANDA
Marketing start
2017-02-23
Marketing end
0000-00-00
Substance
METOPROLOL TARTRATE
Active strength
100 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
68788-6907-9EA - Each68788-6907fcbffdaa-9232-4f7b-97e3-817610607b5012018-08-13