Metoprolol Tartrate

Product NDC
0409-2285
11-digit product format
004092285
Labeler code
0409
Product ID
0409-2285_3be4b7c6-7fa7-458a-b53a-90042e4e8e0f
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
METOPROLOL TARTRATE
Dosage form
INJECTION, SOLUTION
Route
INTRAVENOUS
Labeler
Hospira, Inc.
Application
ANDA075160
Marketing category
ANDA
Marketing start
2006-02-01
Marketing end
0000-00-00
Substance
METOPROLOL TARTRATE
Active strength
1 mg/mL
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

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0409-2285-05ML - Milliliter0409-22856c68ee02-f8b6-4dab-93d9-f536bdd8e98a12012-07-24
0409-2285-15ML - Milliliter0409-22856c46c62f-aafd-483d-af09-d51fa54058a512018-01-12