NDC 51672-1385

Ibuprofen 100 mg per 5 mL suspension

On the label: Caraco Pharmaceutical Laboratories, Ltd..

Where it's made

Recalls

• Sep 27, 2019 · Class II · Taro Pharmaceuticals U.S.A., Inc.
  Presence of Foreign Substance: Ibuprofen Oral Suspension USP may have small particles of an inert plastic material introduced during manufacturing.
  Lots: Lot #: K779030125, Exp 10/19; D873031376, Exp 3/20; J871233188, Exp 9/20; L866934047, Exp 11/20; A973134376, 12/20; D967635229, Exp 3/21
• Sep 27, 2019 · Class II · Taro Pharmaceuticals U.S.A., Inc.
  Presence of Foreign Substance: Ibuprofen Oral Suspension USP may have small particles of an inert plastic material introduced during manufacturing.
  Lots: Lot #: J78402968, J784129698, Exp 9/19; K765129698, K765229698, K765329698, K769329698, K778829698, K778929698, Exp 10/19; A887230568, A887330568, A887430568, Exp 12/19; B865430568, B865530568, B865630568, B869530568, B869630568, Exp 1/20; D866431198, D866531198, D866631198, D866731198, D866831198,…

Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.

Product details

Generic drug

Ibuprofen: every company that makes it

Form

suspension, oral

Strength

100 mg per 5 mL

Approval

ANDA ANDA209204

On the market since

Jun 23, 2017

Package NDCs

51672-1385-8 51672-1385-9

Official label

DailyMed (National Library of Medicine), updated Dec 27, 2025

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