RecallRadar

FDA Drug recall D-0415-2018

Famciclovir Tablets, 500 mg, 30-count bottles, Rx Only, Manufactured For: Camber Pharmaceuticals

On 2018-02-21 the FDA classified a Class II recall of Famciclovir Tablets, 500 mg, 30-count bottles, Rx Only, Manufactured For: Camber Pharmaceuticals by Hetero Labs Unit V, citing temperature Abuse: Complaints of tablets being wet and stuck together with tablet coating peeled and disintegrated as a result of prolonged exposure to high temp during distributi….

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0415-2018
ClassificationClass II
Statusterminated
Initiated2017-12-22
Published2018-02-21
Last updated2026-09-13 11:52 UTC
CompanyHetero Labs Unit V
DistributionUS

Product

Famciclovir Tablets, 500 mg, 30-count bottles, Rx Only, Manufactured For: Camber Pharmaceuticals. Inc. Piscataway, NJ 08854 By: HETERO, Hetero Labs Limited, Unit V, Polepally, Jadcherla, Mahaboob Nagar-509 301, India. NDC 31722-708-30

Reason

Temperature Abuse: Complaints of tablets being wet and stuck together with tablet coating peeled and disintegrated as a result of prolonged exposure to high temp during distribution.

Identifiers

ndc31722-706-30
ndc31722-706-60
ndc31722-706-01
ndc31722-706-05
ndc31722-706-10
ndc31722-707-30
ndc31722-707-60
ndc31722-707-01
ndc31722-707-05
ndc31722-707-10
ndc31722-708-30
ndc31722-708-60
ndc31722-708-01
ndc31722-708-05
ndc31722-708-10
code_infoLot # FMC17039, Exp 07/2019.

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-0415-2018%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.