Ibuprofen

Product NDC
55910-750
11-digit product format
559100750
Labeler code
55910
Product ID
55910-750_b01c67b5-f4b8-4ddb-8ee3-7572a0676d3c
Type
HUMAN OTC DRUG
Nonproprietary name
Ibuprofen
Dosage form
CAPSULE, LIQUID FILLED
Route
ORAL
Labeler
Dolgencorp, Inc. (DOLLAR GENERAL & REXALL)
Application
ANDA206999
Marketing category
ANDA
Marketing start
2018-08-31
Marketing end
2025-01-31
Substance
IBUPROFEN
Active strength
200 mg/1
Pharmacologic classes
Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
55910-750-02559100750021 BOTTLE, PLASTIC in 1 BOX (55910-750-02) > 40 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC2018-08-310000-00-00NoNoCurrent
55910-750-125591007501212 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (55910-750-12) 2018-08-310000-00-00NoNoCurrent
55910-750-20559100750201 BOTTLE, PLASTIC in 1 BOX (55910-750-20) > 20 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC2018-08-310000-00-00NoNoCurrent
55910-750-40559100750401 BOTTLE, PLASTIC in 1 BOX (55910-750-40) > 40 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC2018-08-310000-00-00NoNoCurrent
55910-750-80559100750801 BOTTLE, PLASTIC in 1 BOX (55910-750-80) > 80 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC2018-08-310000-00-00NoNoCurrent