NDC 60760-786

Losartan Potassium 50 mg tablet, film coated

On the label: St. Mary's Medical Park Pharmacy. It's a repackaged product: St. Mary's Medical Park Pharmacy rebottles it from Camber Pharmaceuticals Inc.'s NDC 31722-701.

Where the pills inside were made

Hetero Labs Limited

Mahabubnagar, India · makes it

Problems found, fixed voluntarily Last FDA inspection Aug 12, 2022. 5 inspections on record, 1 with serious problems.

Repackaging site

• St. Mary's Medical Park Pharmacy, Oro Valley, AZ, United States · repackages it and relabels it

Recalls

• Feb 28, 2019 · Class II · Ongoing
  CGMP Deviations; trace amounts of N-Nitroso N-Methyl 4-amino butyric acid (NMBA) detected in the active pharmaceutical ingredient
  Lots: a) LOP17026B, LOP17050, LOP1705, LOP17052, LOP17053, Exp. Sep-19; LOP17061, Exp. Oct-19; LOP18035, LOP18036, Exp. Dec-19; b) LOP17026, Exp. Sep-19; c) LOP17006, Exp. May-19, LOP17025, Exp. Sep-19, LOP17068, Exp, Oct-19, LOP18037, LOP18038, LOP18039, Exp. Dec-19, LOP18057, Exp. Jan-20
• Feb 28, 2019 · Class II · Ongoing
  CGMP Deviations; trace amounts of N-Nitroso N-Methyl 4-amino butyric acid (NMBA) detected in the active pharmaceutical ingredient
  Lots: a) LOP17028C, Exp. Sep-19, LOP17064A, Exp. Nov-19; b) LOP17027, Exp Sep-19, LOP17063, LOP17093, Exp. Nov-19; LOP17094, LOP17095, LOP17097A, LOP17105, LOP17107, Exp. Dec-19; c) LOP17004, Exp Dec-19, LOP17028B, Exp Sep-19, LOP17048, LOP17049 Exp Oct-19, LOP17056, LOP17073, LOP17074, LOP17076 Ex…
• Feb 28, 2019 · Class II · Ongoing
  CGMP Deviations; trace amounts of N-Nitroso N-Methyl 4-amino butyric acid (NMBA) detected in the active pharmaceutical ingredient
  Lots: a) LOP17011, Exp Aug-19, Lot LOP17087 Exp Nov-19; b) LOP17012, LOP17013, Exp Aug-19, LOP17042, LOP17043 Exp Oct-19, LOP17044, LOP17045, Exp Nov-19, LOP18024, LOP18025, LOP18026, LOP18027, LOP18028, LOP18029, LOP18030, Exp. Dec-19; c) LOP17005, Exp May-19, LOP17014, Exp Aug-19, LOP17016, L…

Product details

Generic drug

Losartan: see every company that makes it

Form

tablet, film coated, oral

Strength

50 mg

Approval

ANDA ANDA203835

On the market since

Jul 20, 2020

Package NDCs

60760-786-30 60760-786-90

Official label

DailyMed (National Library of Medicine), updated Jun 7, 2026

Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?