Manufacturers/Greenstone LLC

Greenstone LLC

3 drugs in NADAC|3 Generic,0 Brand

View Recalls (7)

Total Drugs

3

3G / 0B

Avg Price / Unit

$0.8943

$0.19 – $2.31

Avg 7d Change

-0.09%

Across 3 drugs with changes

7d Activity

120 flat

of 3 total drugs

Portfolio Price Trend

Monthly average NADAC price across all drugs

Drug Portfolio

3 drugs total, 3 shown

Drug Price 7d Change
MESALAMINE DR 400 MG CAPSULE
MESALAMINE
$2.3051
per EA
+1.42%
SUCRALFATE 1 GM TABLET
Sucralfate
$0.1889
per EA
-0.84%
SUCRALFATE 1 GM TABLET
Sucralfate
$0.1889
per EA
-0.84%

FDA Recalls (7)

Recalls matched by company name. Verify current status with FDA.

D-0299-2026
Ongoing
Class II

methylprednisolone tablets, USP Dosepak, 4 mg, 1 Blister Card per Carton containing 21 Tablets, Rx only, Distributed by: Greenstone LLC, Peapack, NJ 07977. NDC 59762-4440-2

Labeling: Not Elsewhere Classified. Incorrect orientation of the blister foil applied to the blister cavities, which results in incorrect dosing information when following the directions on the foil.

Initiated: 1/15/2026
D-1361-2014
Terminated
Class I

Venlafaxine HCl Extended-Release Capsules, 150 mg, 90-count Unit of Use bottles, Rx only, Distributed by: Greenstone LLC, Peapack, NJ 07977, NDC 59762-0182-2, UPC 3 59762-0182-2 9.

Presence of Foreign Tablets/Capsules: report of a foreign capsule with markings (TKN 250) and identified as a Tikosyn (dofetilide) capsule was found in a bottle of Effexor XR (venlafaxine HCl) 150 mg capsules that was packaged in the same packaging campaign as the recalled lot

Initiated: 3/6/2014
D-746-2014
Terminated
Class II

sertraline HCl tablets, 25 mg, 30 Tablets, Rx only, GREENSTONE BRAND --- Distributed by: Greenstone LLC, Peapack, NJ 07977 -- MADE IN INDIA --- NDC 59762-4960-1

Labeling: Incorrect or Missing Lot No. and/or Exp Date: Expiration date incorrectly reflects a 36 month shelf life, instead of the 24 month shelf life

Initiated: 11/5/2013
D-1059-2014
Terminated
Class III

Glipizide XL (glipizide) extended release tablets, 5 mg , 500 count bottles, Rx only, Distributed by: Greenstone Ltd., Peapack, NJ --- NDC 59762-5032-2

Failed Dissolution Specification; the bulk lot yielded an out of specification result at the 8 hr timepoint, 18 month interval

Initiated: 11/4/2013
D-737-2014
Terminated
Class II

Nifedipine, extended-release tablets, 90mg 100 count blister pack, Rx only, Distributed by: GREENSTONE LLC, Pespack, NJ,07977, NDC 59762-6692-8

Labeling: Incorrect or Missing Lot and/or Exp Date: Greenstone LLC is recalling Nifedipine Extended Release tablets (90mg). The expiration date on the package is 48 months instead of 36 months.

Initiated: 11/1/2013
D-010-2014
Terminated
Class II

Spironolactone tablets, USP 25 mg, Rx only, 500 count bottle, Distributed By: Greenstone LLC, Peapack, NJ 07977, NDC: 59762-5011-2.

Marketed without an Approved NDA/ANDA: This recall is being initiated because of changes to the dissolution profile in distributed lots resulting from a manufacturing site change. There is currently no approved application supporting the alternate manufacturing site.

Initiated: 9/4/2013
D-011-2014
Terminated
Class II

Spironolactone tablets, USP 50 mg, Rx only, 100 count bottle, Distributed By: Greenstone LLC, Peapack, NJ 07977, NDC: 59762-5012-1

Marketed without an Approved NDA/ANDA: This recall is being initiated because of changes to the dissolution profile in distributed lots resulting from a manufacturing site change. There is currently no approved application supporting the alternate manufacturing site.

Initiated: 9/4/2013