RecallRadar

FDA Drug recall D-1032-2020

Doxycycline Capsules, USP, 75 mg, 100-count bottle, Rx only, Manufactured by: Ohm Laboratories Inc., New Brunswick, NJ 08901

On 2020-03-25 the FDA classified a Class II recall of Doxycycline Capsules, USP, 75 mg, 100-count bottle, Rx only, Manufactured by: Ohm Laboratories Inc., New Brunswick, NJ 08901 by Sun Pharmaceutical Industries, citing CGMP Deviations: Doxycycline capsules were not manufactured under Current Good Manufacturing Practice conditions.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-1032-2020
ClassificationClass II
Statusterminated
Initiated2020-03-13
Published2020-03-25
Last updated2026-09-13 11:52 UTC
CompanySun Pharmaceutical Industries
DistributionUS

Product

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.

Reason

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

Identifiers

ndc63304-614-20
ndc63304-614-05
ndc63304-614-01
ndc63304-614-13
ndc63304-615-05
ndc63304-615-11
ndc63304-615-01
ndc63304-616-20
ndc63304-616-05
ndc63304-616-01
ndc63304-616-13
ndc63304-616-50
code_infoLot #: AA39490, Exp 03/2021

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1032-2020%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.