Ibuprofen

Product NDC
66689-339
11-digit product format
666890339
Labeler code
66689
Product ID
66689-339_26b551dc-ca1d-409f-a284-40237694784e
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Ibuprofen
Dosage form
SUSPENSION
Route
ORAL
Labeler
VistaPharm, Inc.
Application
ANDA074978
Marketing category
ANDA
Marketing start
2019-02-01
Marketing end
0000-00-00
Substance
IBUPROFEN
Active strength
100 mg/5mL
Pharmacologic classes
Cyclooxygenase Inhibitors [MoA],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
66689-339-01ML - Milliliter66689-33991f1eff6-7049-4da6-ba02-0db7dca4822012019-04-11
66689-339-50ML - Milliliter66689-3390a603e30-2ae2-4342-91d6-43187bff12ee12019-04-11

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
66689-339-50666890339505 TRAY in 1 CASE (66689-339-50) > 10 CUP, UNIT-DOSE in 1 TRAY > 5 mL in 1 CUP, UNIT-DOSE (66689-339-01) 5 tray2019-02-010000-00-00NoNoCurrent