Flurbiprofen Sodium

Product NDC
50090-0625
11-digit product format
500900625
Labeler code
50090
Product ID
50090-0625_f32d7200-089a-4e51-9142-0cde2e1b2144
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Flurbiprofen Sodium
Dosage form
SOLUTION/ DROPS
Route
OPHTHALMIC
Labeler
A-S Medication Solutions
Application
ANDA074447
Marketing category
ANDA
Marketing start
1995-01-04
Marketing end
0000-00-00
Substance
FLURBIPROFEN SODIUM
Active strength
0 mg/mL
Pharmacologic classes
Cyclooxygenase Inhibitors [MoA],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [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
50090-0625-0ML - Milliliter50090-0625324631aa-b971-4867-ae8d-bdeda16fd02112018-09-05