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Drug company (FDA labeler)

Lifestar Pharma LLC

NDC labeler code: 70756

What is a labeler?

The company whose name is on the package and in the FDA’s National Drug Code (NDC) Directory. It may make the medicine itself or sell medicine made by another company. The first part of every NDC code identifies the labeler.

Official FDA data only

Products, approvals and recalls come from the FDA (NDC Directory, Drugs@FDA, enforcement reports). Recalls are linked to this company by the NDC labeler code on the recalled product.

Questions about your medicine: ask your doctor or pharmacist. In an emergency, call 911.

At a glance

159Products (NDC)

Prescription medicines

Show the other 17 medicines

FDA applications for these products

  • NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
  • ANDA: Abbreviated New Drug Application: how a generic version is approved.
ApprovedApplicationMedicineSponsor
July 31, 2026ANDA220513 Thiamine hydrochloride
THIAMINE HYDROCHLORIDE
Mankind Pharma
July 1, 2026ANDA220874 Rivaroxaban
RIVAROXABAN
Mankind Pharma
April 16, 2026ANDA220398 Brimonidine tartrate
BRIMONIDINE TARTRATE
Mankind Pharma
February 6, 2026ANDA217679 Ticagrelor
TICAGRELOR
Mankind Pharma
January 27, 2026ANDA216663 Propranolol hydrochloride
PROPRANOLOL HYDROCHLORIDE
Mankind Pharma
December 17, 2025ANDA220360 Latanoprost
LATANOPROST
Mankind Pharma
August 12, 2025ANDA217358 Divalproex sodium
DIVALPROEX SODIUM
Mankind Pharma
May 29, 2025ANDA219674 Rocuronium bromide
ROCURONIUM BROMIDE
Mankind Pharma
May 21, 2025ANDA219136 Proparacaine hydrochloride
PROPARACAINE HYDROCHLORIDE
Mankind Pharma
May 16, 2025ANDA206603 Rosuvastatin
ROSUVASTATIN CALCIUM
Mankind Pharma
April 3, 2025ANDA219291 Bumetanide
BUMETANIDE
Mankind Pharma
March 17, 2025ANDA218196 Bimatoprost
BIMATOPROST
Mankind Pharma
March 3, 2025ANDA218406 Telmisartan and hydrochlorothiazide
TELMISARTAN AND HYDROCHLOROTHIAZIDE
Mankind Pharma
January 27, 2025ANDA217988 Moxifloxacin
MOXIFLOXACIN HYDROCHLORIDE
Mankind Pharma
October 15, 2024ANDA218157 Telmisartan
TELMISARTAN
Mankind Pharma
July 10, 2024ANDA217839 Cyanocobalamin
CYANOCOBALAMIN
Mankind Pharma
April 11, 2024ANDA216918 Haloperidol
HALOPERIDOL
Mankind Pharma
February 29, 2024ANDA218404 Naloxone hydrochloride
NALOXONE HYDROCHLORIDE
Mankind Pharma
January 8, 2024ANDA218148 Atropine
ATROPINE SULFATE
Mankind Pharma
January 5, 2024ANDA217081 Atorvastatin
ATORVASTATIN CALCIUM
Mankind Pharma
December 5, 2023ANDA217970 Nitroglycerin
NITROGLYCERIN
Mankind Pharma
November 1, 2023ANDA217271 Midodrine hydrochloride
MIDODRINE HYDROCHLORIDE
Mankind Pharma
July 11, 2023ANDA217357 Nitrofurantoin (monohydrate/macrocrystals)
NITROFURANTOIN (MONOHYDRATE/MACROCRYSTALS)
Mankind Pharma
July 11, 2023ANDA217693 Lidocaine
LIDOCAINE HYDROCHLORIDE
Mankind Pharma
June 30, 2023ANDA214478 Tobramycin
TOBRAMYCIN
Mankind Pharma
Show the other 37 applications
ApprovedApplicationMedicineSponsor
June 16, 2023ANDA217692 Lidocaine
LIDOCAINE HYDROCHLORIDE
Mankind Pharma
May 23, 2023ANDA216730 Haloperidol decanoate
HALOPERIDOL DECANOATE
Mankind Pharma
March 22, 2023ANDA215883 Formoterol fumarate
FORMOTEROL FUMARATE
Mankind Pharma
March 21, 2023ANDA217272 Nitrofurantoin
NITROFURANTOIN
Mankind Pharma
February 27, 2023ANDA217354 Glycopyrrolate
GLYCOPYRROLATE
Mankind Pharma
February 2, 2023ANDA216127 Succinylcholine
SUCCINYLCHOLINE CHLORIDE
Mankind Pharma
January 11, 2023ANDA216496 Phenylephrine
PHENYLEPHRINE HYDROCHLORIDE
Mankind Pharma
December 30, 2022ANDA215697 Prazosin hydrochloride
PRAZOSIN HYDROCHLORIDE
Mankind Pharma
December 16, 2022ANDA216860 Furosemide
FUROSEMIDE
Mankind Pharma
November 23, 2022ANDA215886 Ofloxacin
OFLOXACIN
Mankind Pharma
November 15, 2022ANDA216128 Arformoterol tartrate
ARFORMOTEROL TARTRATE
Mankind Pharma
November 14, 2022ANDA216172 Nebivolol
NEBIVOLOL HYDROCHLORIDE
Mankind Pharma
September 29, 2022ANDA216859 Phenylephrine
PHENYLEPHRINE HYDROCHLORIDE
Mankind Pharma
September 22, 2022ANDA216725 Tobramycin
TOBRAMYCIN
Mankind Pharma
August 30, 2022ANDA217069 Phenylephrine
PHENYLEPHRINE HYDROCHLORIDE
Mankind Pharma
August 4, 2022ANDA215587 Chlorthalidone
CHLORTHALIDONE
Mankind Pharma
July 26, 2022ANDA215880 Pantoprazole sodium
PANTOPRAZOLE SODIUM
Mankind Pharma
July 14, 2022ANDA216130 Ofloxacin
OFLOXACIN
Mankind Pharma
June 15, 2022ANDA214653 Verapamil hydrochloride
VERAPAMIL HYDROCHLORIDE
Mankind Pharma
April 14, 2022ANDA216129 Ephedrine sulfate
EPHEDRINE SULFATE
Mankind Pharma
February 9, 2022ANDA215710 Doxepin hydrochloride
DOXEPIN HYDROCHLORIDE
Mankind Pharma
January 25, 2022ANDA215885 Baclofen
BACLOFEN
Mankind Pharma
November 15, 2021ANDA215458 OMEGA-3-ACID ethyl esters
OMEGA-3-ACID ETHYL ESTERS
Mankind Pharma
February 19, 2021ANDA213999 Amitriptyline hydrochloride
AMITRIPTYLINE HYDROCHLORIDE
Mankind Pharma
October 7, 2020ANDA214282 Acetazolamide
ACETAZOLAMIDE
Mankind Pharma
September 9, 2020ANDA213614 Alosetron hydrochloride
ALOSETRON HYDROCHLORIDE
Mankind Pharma
June 12, 2020ANDA213864 Fenofibrate
FENOFIBRATE
Mankind Pharma
April 27, 2020ANDA211724 Capecitabine
CAPECITABINE
Somerset Theraps LLC
February 12, 2020ANDA212284 Ranolazine
RANOLAZINE
Mankind Pharma
September 17, 2019ANDA208847 Olmesartan medoxomil and hydrochlorothiazide
OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE
Pharmazone
July 18, 2019ANDA207135 Olmesartan medoxomil
OLMESARTAN MEDOXOMIL
Pharmazone
April 8, 2019ANDA211767 Clomipramine hydrochloride
CLOMIPRAMINE HYDROCHLORIDE
Mankind Pharma
August 30, 2017ANDA205868 Lansoprazole
LANSOPRAZOLE
Adaptis
November 10, 2011NDA022497 Bupropion
FORFIVO XL
Twi Pharms
November 17, 2009ANDA090671 Nicardipine
NICARDIPINE HYDROCHLORIDE
Mankind Pharma
September 28, 2009ANDA078771 Timolol
TIMOLOL MALEATE
Mankind Pharma
April 16, 2001ANDA075302 Famotidine
FAMOTIDINE
Mankind Pharma

The sponsor is the company that holds the FDA application; it can differ from the labeler.

Recall timeline

No recall of these products (by NDC code) appears in the FDA enforcement reports.

Sources

  1. NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  2. Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  3. Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026

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