NDC 63004-8710

Acthar

Repository Corticotropin

Acthar is a Intramuscular; Subcutaneous Injection in the Human Prescription Drug category. It is labeled and distributed by Mallinckrodt Ard Llc. The primary component is Corticotropin.

Product ID63004-8710_1716c3dd-83e8-4ec0-91d2-965e54b04f6f
NDC63004-8710
Product TypeHuman Prescription Drug
Proprietary NameActhar
Generic NameRepository Corticotropin
Dosage FormInjection
Route of AdministrationINTRAMUSCULAR; SUBCUTANEOUS
Marketing Start Date2013-01-07
Marketing CategoryNDA / NDA
Application NumberNDA022432
Labeler NameMallinckrodt ARD LLC
Substance NameCORTICOTROPIN
Active Ingredient Strength80 [USP'U]/mL
Pharm ClassesAdrenocorticotropic Hormone [CS],Adrenocorticotropic Hormone [EPC]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 63004-8710-1

1 VIAL, MULTI-DOSE in 1 CARTON (63004-8710-1) > 5 mL in 1 VIAL, MULTI-DOSE
Marketing Start Date2013-01-07
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 63004-8710-2 [63004871002]

Acthar INJECTION
Marketing CategoryNDA
Application NumberNDA022432
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2013-01-07

NDC 63004-8710-1 [63004871001]

Acthar INJECTION
Marketing CategoryNDA
Application NumberNDA022432
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2013-01-07

NDC 63004-8710-3 [63004871003]

Acthar INJECTION
Marketing CategoryNDA
Application NumberNDA022432
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2013-01-07

Drug Details

Pharmacological Class

  • Adrenocorticotropic Hormone [CS]
  • Adrenocorticotropic Hormone [EPC]

NDC Crossover Matching brand name "Acthar" or generic name "Repository Corticotropin"

NDCBrand NameGeneric Name
63004-8710ActharRepository Corticotropin
62559-860Purified Cortrophin GelRepository Corticotropin

Trademark Results [Acthar]

Mark Image

Registration | Serial
Company
Trademark
Application Date
ACTHAR
ACTHAR
78649502 3093264 Live/Registered
MALLINCKRODT ARD IP LIMITED
2005-06-13
ACTHAR
ACTHAR
71606253 0563816 Dead/Expired
ARMOUR AND COMPANY
1950-11-13

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.