NDC 70518-4595
Ibuprofen 100 mg per 5 mL suspension
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Caraco Pharmaceutical Laboratories, Ltd.'s NDC 51672-1385.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Sun Pharma Canada Inc. | Brampton, Canada | Makes it | No problems foundMar 27, 2026 · 7 inspections |
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
- Mar 24, 2026
- Package NDCs
70518-4595-0- Official label
- DailyMed (National Library of Medicine), updated Mar 24, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?