Data Foundry

Drug recalls 2015

Azithromycin Tablets — Class II drug recall D-1263-2015

Terminated recall by Wockhardt Usa Inc., reported 2015-07-29, distributed nationwide. CGMP Deviations: Firm did not adequately investigate customer complaints.

Recall numberD-1263-2015
Product typeDrug
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmWockhardt Usa Inc., Parsippany, NJ, United States
Recall initiated2015-04-22
Classified2015-07-17
Reported by FDA2015-07-29
Terminated2018-05-09
DistributedNationwide (US)
Reason classescgmp
NDC64679-0964-01, 64679-0964-05
Lot numbersLM10739, LM10991, LM11015, LM11264, LM11609, LM11883, LM11918, LM12019, LN10100, LN10220, LN10227, LN10228, LN10274, LN11045, LN11327, LN11332, LN11405
Expiration dates2015-04-30, 2015-05-31, 2015-06-30, 2015-09-30, 2015-10-31, 2015-11-30, 2015-12-31, 2016-04-30, 2016-07-31, 2016-09-30

Product

Azithromycin Tablets, USP, 500 mg Tablets, Packaged in A) 30 Count Bottles (NDC: 64679-0964-01) and B) 3 x 3 Tablet Card Cartons (NDC: 64679-964-05), Rx only. Manufactured by: Wockhardt Limited, Mumbai, India. Distributed by: Wockhardt USA LLC 20 Waterview Blvd. Parsippany, NJ 07054 USA.

Reason for recall

CGMP Deviations: Firm did not adequately investigate customer complaints.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-1263-2015. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.