RecallRadar

FDA Drug recall D-0087-2023

Glycopyrrolate Tablets, USP, 1 mg, 100 tablets, Rx Only, Distributed by: Aurobindo Pharma USA, Inc., East Windsor, NJ 08520, NDC 13107-014-…

On 2022-12-28 the FDA classified a Class II recall of Glycopyrrolate Tablets, USP, 1 mg, 100 tablets, Rx Only, Distributed by: Aurobindo Pharma USA, Inc., East Windsor, NJ 08520, NDC 13107-014-… by Aurolife Pharma, citing failed Impurities/Degradation Specifications.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0087-2023
ClassificationClass II
Statusongoing
Initiated2022-12-16
Published2022-12-28
Last updated2026-09-13 11:52 UTC
CompanyAurolife Pharma
DistributionUS

Product

Glycopyrrolate Tablets, USP, 1 mg, 100 tablets, Rx Only, Distributed by: Aurobindo Pharma USA, Inc., East Windsor, NJ 08520, NDC 13107-014-01

Reason

Failed Impurities/Degradation Specifications

Identifiers

ndc13107-014-01
ndc13107-015-01
code_infoLots: 01422002A1, Expiry: 12/2023; 01421078A3, Expiry: 09/2023

Status history

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

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0087-2023%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.