NDC 0009-0039

SOLU-MEDROL

Methylprednisolone Sodium Succinate

SOLU-MEDROL is a Intramuscular; Intravenous Injection, Powder, For Solution in the Human Prescription Drug category. It is labeled and distributed by Pharmacia And Upjohn Company Llc. The primary component is Methylprednisolone Sodium Succinate.

• Product ID: 0009-0039_2037261b-cc7a-42a2-af8e-7c8e7dc2d894
• NDC: 0009-0039
• Product Type: Human Prescription Drug
• Proprietary Name: SOLU-MEDROL
• Generic Name: Methylprednisolone Sodium Succinate
• Dosage Form: Injection, Powder, For Solution
• Route of Administration: INTRAMUSCULAR; INTRAVENOUS
• Marketing Start Date: 1959-04-02
• Marketing Category: NDA / NDA
• Application Number: NDA011856
• Labeler Name: Pharmacia and Upjohn Company LLC
• Substance Name: METHYLPREDNISOLONE SODIUM SUCCINATE
• Active Ingredient Strength: 40 mg/mL
• Pharm Classes: Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
• NDC Exclude Flag: N
• Listing Certified Through: 2021-12-31

Packaging

NDC 0009-0039-06

25 VIAL in 1 CARTON (0009-0039-06) > 1 mL in 1 VIAL

• Marketing Start Date: 1959-04-02
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0009-0039-06 [00009003906]

SOLU-MEDROL INJECTION, POWDER, FOR SOLUTION

• Marketing Category: NDA
• Application Number: NDA011856
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1959-04-02

NDC 0009-0039-33 [00009003933]

SOLU-MEDROL INJECTION, POWDER, FOR SOLUTION

• Marketing Category: NDA
• Application Number: NDA011856
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1959-04-02

NDC 0009-0039-32 [00009003932]

SOLU-MEDROL INJECTION, POWDER, FOR SOLUTION

• Marketing Category: NDA
• Application Number: NDA011856
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1959-04-02

NDC 0009-0039-30 [00009003930]

SOLU-MEDROL INJECTION, POWDER, FOR SOLUTION

• Marketing Category: NDA
• Application Number: NDA011856
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2012-08-27

NDC 0009-0039-28 [00009003928]

SOLU-MEDROL INJECTION, POWDER, FOR SOLUTION

• Marketing Category: NDA
• Application Number: NDA011856
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1959-04-02

Drug Details

Active Ingredients

Ingredient	Strength
METHYLPREDNISOLONE SODIUM SUCCINATE	40 mg/mL

OpenFDA Data

• SPL SET ID: cd99be87-c8d9-48d6-a8e5-e081052e3f19
• Manufacturer:
  • Pharmacia and Upjohn Company LLC
• UNII:
  • LEC9GKY20K
• RxNorm Concept Unique ID - RxCUI:
  • 1743729
  • 311659
  • 1743720
  • 314099
  • 1743726
  • 1743704
  • 1743707
  • 1357888
  • 1357886
  • 207193
  • 207191
  • 1743722
• UPC Code:
  • 0300090758011
  • 0300090018207
  • 0300090003029
  • 0300090698010

Pharmacological Class

• Corticosteroid [EPC]
• Corticosteroid Hormone Receptor Agonists [MoA]

NDC Crossover Matching brand name "SOLU-MEDROL" or generic name "Methylprednisolone Sodium Succinate"

NDC	Brand Name	Generic Name
0009-0003	SOLU-MEDROL	methylprednisolone sodium succinate
0009-0018	SOLU-MEDROL	methylprednisolone sodium succinate
0009-0039	SOLU-MEDROL	methylprednisolone sodium succinate
0009-0047	SOLU-MEDROL	methylprednisolone sodium succinate
0009-0698	SOLU-MEDROL	methylprednisolone sodium succinate
68071-1792	SOLU-MEDROL	SOLU-MEDROL
70385-2016	SOLU-MEDROL	SOLU-MEDROL
70518-0334	SOLU-MEDROL	SOLU-MEDROL
70518-1424	SOLU-MEDROL	SOLU-MEDROL
71872-7061	SOLU-MEDROL	SOLU-MEDROL
0009-0758	SOLU-MEDROL	SOLU-MEDROL
0009-0796	Solu-Medrol	Solu-Medrol
50090-0271	SOLU-MEDROL	SOLU-MEDROL
51662-1263	SOLU-MEDROL	SOLU-MEDROL
51662-1264	SOLU-MEDROL	SOLU-MEDROL
52584-039	Solu-Medrol	Solu-Medrol
52584-047	Solu-Medrol	Solu-Medrol
55154-3939	Solu-Medrol	Solu-Medrol
55154-3941	Solu-Medrol	Solu-Medrol
55154-3940	Solu-Medrol	Solu-Medrol
55154-3944	Solu-Medrol	Solu-Medrol
61699-0047	SOLU-MEDROL	SOLU-MEDROL
70518-2023	SOLU-MEDROL	SOLU-MEDROL
0009-0850	SOLU-MEDROL	SOLU-MEDROL