HUMULIN

This brand name is authorized in Australia, Brazil, Canada, Cyprus, Germany, Ecuador, Estonia, Finland, Hong Kong, Croatia, Ireland, Israel, Japan, Lithuania, Malta, Nigeria, New Zealand, Poland, Romania, Singapore, Turkey, United Kingdom, United States, South Africa

Active ingredients

The drug HUMULIN contains one active pharmaceutical ingredient (API):

1 Insulin (human)
UNII 1Y17CTI5SR - INSULIN HUMAN

The blood glucose lowering effect of insulin is due to the facilitated uptake of glucose following binding of insulin to receptors on muscle and fat cells and to the simultaneous inhibition of glucose output from the liver.

Read about Insulin (human)

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
HUMULIN I Suspension for injection in a vial Medicines & Healthcare Products Regulatory Agency (GB) MPI, EU: SmPC

Medicine classification

This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:

ATC code Group title Classification
A10AB01 Insulin (human) A Alimentary tract and metabolism → A10 Drugs used in diabetes → A10A Insulins and analogues → A10AB Insulins and analogues for injection, fast-acting
Discover more medicines within A10AB01
A10AC01 Insulin (human) A Alimentary tract and metabolism → A10 Drugs used in diabetes → A10A Insulins and analogues → A10AC Insulins and analogues for injection, intermediate-acting
Discover more medicines within A10AC01
A10AD01 Insulin (human) A Alimentary tract and metabolism → A10 Drugs used in diabetes → A10A Insulins and analogues → A10AD Insulins and analogues for injection, intermediate-acting combined with fast-acting
Discover more medicines within A10AD01

Authorization and marketing

This drug has been assigned below unique identifiers within the countries it is being marketed:

Country Identification scheme Identifier(s)
Country: AU Pharmaceutical Benefits Scheme Identifier(s): 1426C, 1531N, 1533Q, 1761Q, 1762R, 1763T
Country: BR Câmara de Regulação do Mercado de Medicamentos Identifier(s): 507601613154412, 507601614150410, 507604502159410, 507604503155419, 507604602153414, 507604603151415
Country: CA Health Products and Food Branch Identifier(s): 00586714, 00587737, 00795879, 01959212, 01959220, 01959239, 02403447, 02415089
Country: DE Bundesinstitut für Arzneimittel und Medizinprodukte Identifier(s): 00066789, 00927292, 02406462, 02406479, 02815717, 02817573, 02817604, 02817610, 03382947, 03383912, 03386678, 03386684, 04681882, 04681899, 05917157, 06079072, 06080253, 06577114, 06577120, 07121126, 07121385, 07749801, 07749818, 07759998, 07760004, 09534306, 11540662, 11540679, 12893397, 12893405, 13588839, 13588845, 13978948, 13978954, 16944223, 16944246
Country: EC Agencia Nacional de Regulación, Control y Vigilancia Sanitaria Identifier(s): 25.542-01-04, 29355-09-10, 29357-09-10, 29358-09-10
Country: EE Ravimiamet Identifier(s): 1029417, 1115615, 1115637, 1745030, 1745052, 1745074, 1745085
Country: FI Lääkealan turvallisuus- ja kehittämiskeskus Identifier(s): 532390
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 156032, 175592, 175594, 176087, 176097, 179000, 180490, 196144, 32560, 32643, 32738, 32749, 33114, 33127, 352144, 352145, 374171, 374173, 374200, 374205, 377198, 381396, 381398, 381400, 391006, 396486, 399392
Country: HK Department of Health Drug Office Identifier(s): 26619, 26623, 39494, 39495, 39509, 47649, 62311, 62312
Country: HR Agencija za lijekove i medicinske proizvode Identifier(s): HR-H-162520244, HR-H-382405435, HR-H-423917539
Country: IE Health Products Regulatory Authority Identifier(s): 69069, 69077, 69100, 69137, 69169, 69183, 69312, 69337
Country: IL מִשְׂרַד הַבְּרִיאוּת Identifier(s): 3317, 3321, 3322, 734, 735
Country: JP 医薬品医療機器総合機構 Identifier(s): 2492403A3047, 2492403A4051, 2492403H1034, 2492403H4041, 2492403H5030, 2492403H6036, 2492413G9025, 2492413P1024, 2492413P2020
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1004375, 1004379, 1004380, 1004381, 1004383, 1076847, 1076848, 1076849, 1076850, 1076851, 1084884, 1084885, 1084886, 1084887, 1084888, 1084889, 1084890
Country: MT Medicines Authority Identifier(s): MA637/00304, MA637/00305, MA637/00306
Country: NG Registered Drug Product Database Identifier(s): A6-0149, A6-0270, A6-0271
Country: NZ Medicines and Medical Devices Safety Authority Identifier(s): 3889, 3895, 3900
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100029621, 100091940, 100193970
Country: RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale Identifier(s): W52986002, W52986003, W52999001, W52999002, W52999003, W52999004, W52999005, W53106002, W53106003, W64794001, W64794002, W64794003, W64795001, W64795002, W64795003, W64796001, W64796002, W64796003
Country: SG Health Sciences Authority Identifier(s): 04286P, 04354P, 06019P, 07574P, 07581P, 07684P
Country: TR İlaç ve Tıbbi Cihaz Kurumu Identifier(s): 8699673774206, 8699673774213, 8699673954158, 8699673954165, 8699673954172
Country: US FDA, National Drug Code Identifier(s): 0002-8501, 0002-8824
Country: ZA Health Products Regulatory Authority Identifier(s): R/21.1/0001, R/21.1/0002

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