Metoprolol Tartrate

Product NDC
55700-667
11-digit product format
557000667
Labeler code
55700
Product ID
55700-667_e34ad132-3cf2-462b-8610-3bf3e7733371
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Metoprolol Tartrate
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Lake Erie Medical DBA Quality Care Products LLC
Application
ANDA200981
Marketing category
ANDA
Marketing start
2018-08-10
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
2020-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
55700-667-30EA - Each55700-667c3022099-1d28-4d28-bd94-de0e24c686ea12019-05-02
55700-667-60EA - Each55700-667d6827ea6-a446-4a28-a0cb-0be33fdd561e12018-09-05
55700-667-90EA - Each55700-66745b89417-7dcc-4058-9aec-b2210c5ff3a712018-09-05