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Class II: temporary or reversible health riskTerminated

Sun Pharmaceutical Industries Doxycycline Capsules Recall

Doxycycline Capsules, USP, 75 mg, 100-count bottle, Rx only, Manufactured by: Ohm Labor…

Sun Pharmaceutical Industries, Inc. · Cranbury, NJ

Risk level
Class II
Reported by FDA
Mar 25, 2020
Recall ID
D-1032-2020
Check your lot numberHow we source this data

Summary

Sun Pharmaceutical Industries recalled Doxycycline Capsules starting Mar 13, 2020. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-1032-2020 on Mar 25, 2020. Reason: CGMP Deviations: Doxycycline capsules were not manufactured under Current Good Manufacturing Practice conditions. Status: Terminated.

Why it was recalled

CGMP Deviations: Doxycycline capsules were not manufactured under Current Good Manufacturing Practice conditions.

Product description

Doxycycline Capsules, USP, 75 mg, 100-count bottle, Rx only, Manufactured by: Ohm Laboratories Inc., New Brunswick, NJ 08901; Distributed by Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512; NDC 63304-615-01.

Lot numbers, UPCs & expiration codes

Lot #: AA39490, Exp 03/2021

Where it was sold

Nationwide in the USA

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-1032-2020
Classification
Class II
Status
Terminated
Recall initiated
Mar 13, 2020
FDA report date
Mar 25, 2020
Quantity
624 bottles
Recall type
Voluntary: Firm initiated
Recalling firm
Sun Pharmaceutical Industries, Inc.

Original FDA data

Every field from FDA enforcement report D-1032-2020, exactly as published.

Show all FDA fields
City
Cranbury
State
NJ
Status
Terminated
Country
United States
Event ID
85230
Address
270 Prospect Plains Rd
Code information
Lot #: AA39490, Exp 03/2021
Postal code
08512-3605
Report date
Mar 25, 2020
Product type
Drugs
Recall number
D-1032-2020
Classification
Class II
Recalling firm
Sun Pharmaceutical Industries, Inc.
Product quantity
624 bottles
Termination date
Feb 9, 2021
Reason for recall
CGMP Deviations: Doxycycline capsules were not manufactured under Current Good Manufacturing Practice conditions.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Doxycycline Capsules, USP, 75 mg, 100-count bottle, Rx only, Manufactured by: Ohm Laboratories Inc., New Brunswick, NJ 08901; Distributed by Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512; NDC 63304-615-01.
Distribution pattern
Nationwide in the USA
Recall initiation date
Mar 13, 2020
Initial firm notification
Letter
Center classification date
Mar 18, 2020

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1032-2020, published Mar 25, 2020. View the source record (openFDA) · FDA enforcement reports

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

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

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