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Class II: temporary or reversible health riskTerminated

Time-Cap Laboratories Ibuprofen Tablets 600 mg Recall

Ibuprofen Tablets USP 600 mg, a) 100 tablet (NDC 49483-603-01) and b) 500 tablet bottle…

Time-Cap Laboratories, Inc. · Farmingdale, NY

Risk level
Class II
Reported by FDA
May 2, 2018
Recall ID
D-0689-2018
Check your lot numberHow we source this data

Summary

Time-Cap Laboratories recalled Ibuprofen Tablets 600 mg starting Jan 11, 2018. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0689-2018 on May 2, 2018. Reason: CGMP Deviations: Various strengths of ibuprofen tablets/caplets are being recalled due to complaints of odor related to CGMP deficiencies. Status: Terminated.

Why it was recalled

CGMP Deviations: Various strengths of ibuprofen tablets/caplets are being recalled due to complaints of odor related to CGMP deficiencies.

Product description

Ibuprofen Tablets USP 600 mg, a) 100 tablet (NDC 49483-603-01) and b) 500 tablet bottles (NDC 49483-603-50), Rx, Manufactured for: Time Caps Labs, Farmingdale, NY, Manufactured by: Marksans Pharma, Ltd., Plot No. L-82, L-83 Verna indl. Estate Verna, Goa-403 722, India

Lot numbers, UPCs & expiration codes

a) C135C, D044C, D045C, D038C, exp 3/18, F069C, exp 4/18, H095C, exp 9/18 b) C134C, C136C, D039C, D040C, D041C, D042C, D043C, exp 3/18, F043C F067C, F068C, D046C, D047C, exp 4/18, H094C, exp 7/18 H096C, L026C, and H095C, exp 9/18

Where it was sold

Nationwide.

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-0689-2018
Classification
Class II
Status
Terminated
Recall initiated
Jan 11, 2018
FDA report date
May 2, 2018
Quantity
N/A
Recall type
Voluntary: Firm initiated
Recalling firm
Time-Cap Laboratories, Inc.

Original FDA data

Every field from FDA enforcement report D-0689-2018, exactly as published.

Show all FDA fields
City
Farmingdale
State
NY
Status
Terminated
Country
United States
Event ID
79349
Address
7 Michael Ave
Code information
a) C135C, D044C, D045C, D038C, exp 3/18, F069C, exp 4/18, H095C, exp 9/18 b) C134C, C136C, D039C, D040C, D041C, D042C, D043C, exp 3/18, F043C F067C, F068C, D046C, D047C, exp 4/18, H094C, exp 7/18 H096C, L026C, and H095C, exp 9/18
Postal code
11735-3921
Report date
May 2, 2018
Product type
Drugs
Recall number
D-0689-2018
Classification
Class II
Recalling firm
Time-Cap Laboratories, Inc.
Termination date
Jan 20, 2021
Reason for recall
CGMP Deviations: Various strengths of ibuprofen tablets/caplets are being recalled due to complaints of odor related to CGMP deficiencies.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Ibuprofen Tablets USP 600 mg, a) 100 tablet (NDC 49483-603-01) and b) 500 tablet bottles (NDC 49483-603-50), Rx, Manufactured for: Time Caps Labs, Farmingdale, NY, Manufactured by: Marksans Pharma, Ltd., Plot No. L-82, L-83 Verna indl. Estate Verna, Goa-403 722, India
Distribution pattern
Nationwide.
Recall initiation date
Jan 11, 2018
Initial firm notification
Letter
Center classification date
Apr 22, 2018

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0689-2018, published May 2, 2018. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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