RecallRadar

FDA Drug recall D-1214-2018

Morphine Sulfate Extended-Release Tablets, 30 mg, 100-count bottle, Rx only, Manufactured by: Novel Laboratories, Inc

On 2018-09-26 the FDA classified a Class III recall of Morphine Sulfate Extended-Release Tablets, 30 mg, 100-count bottle, Rx only, Manufactured by: Novel Laboratories, Inc by Lupin Somerset, citing failed Impurities/Degradation Specifications: Morphine Sulfate Extended Release Tablets are being recalled due to out of Specification Result noticed for Morphinone Sulfate impuri….

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-1214-2018
ClassificationClass III
Statusterminated
Initiated2018-08-23
Published2018-09-26
Last updated2026-09-13 11:52 UTC
CompanyLupin Somerset
DistributionUS

Product

Morphine Sulfate Extended-Release Tablets, 30 mg, 100-count bottle, Rx only, Manufactured by: Novel Laboratories, Inc. Somerset, NJ 08873, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, MD 21202, NDC 43386-541-01

Reason

Failed Impurities/Degradation Specifications: Morphine Sulfate Extended Release Tablets are being recalled due to out of Specification Result noticed for Morphinone Sulfate impurity during 3 month stability analysis and during retain testing.

Identifiers

ndc43386-540-01
ndc43386-540-05
ndc43386-541-01
ndc43386-541-05
ndc43386-542-01
ndc43386-542-05
ndc43386-543-01
ndc43386-543-05
ndc43386-544-01
ndc43386-544-05
code_infoLot# S800232, Exp 2/20

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-1214-2018%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.