NDC 67467-623

Albumin (Human)

Albumin Human

Albumin (Human) is a Intravenous Solution in the Human Prescription Drug category. It is labeled and distributed by Octapharma Pharmazeutika Produktionsgesellschaft M.b.h.. The primary component is Albumin (human).

• Product ID: 67467-623_0115cedc-4781-0619-f8c9-82e8199df443
• NDC: 67467-623
• Product Type: Human Prescription Drug
• Proprietary Name: Albumin (Human)
• Generic Name: Albumin Human
• Dosage Form: Solution
• Route of Administration: INTRAVENOUS
• Marketing Start Date: 2006-10-17
• Marketing Category: BLA / BLA
• Application Number: BLA125154
• Labeler Name: Octapharma Pharmazeutika Produktionsgesellschaft m.b.H.
• Substance Name: ALBUMIN (HUMAN)
• Active Ingredient Strength: 50 g/1000mL
• Pharm Classes: Human Serum Albumin [EPC],Increased Intravascular Volume [PE],Increased Oncotic Pressure [PE],Osmotic Activity [MoA],Serum Albumin [Chemical/Ingredient]
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 67467-623-03

500 mL in 1 BOTTLE, GLASS (67467-623-03)

• Marketing Start Date: 2006-10-17
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 67467-623-01 [67467062301]

Albumin (Human) SOLUTION

• Marketing Category: BLA
• Application Number: BLA125154
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: ML
• Marketing Start Date: 2006-10-17
• Inactivation Date: 2019-10-21

NDC 67467-623-03 [67467062303]

Albumin (Human) SOLUTION

• Marketing Category: BLA
• Application Number: BLA125154
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: ML
• Marketing Start Date: 2006-10-17
• Inactivation Date: 2019-10-21

NDC 67467-623-02 [67467062302]

Albumin (Human) SOLUTION

• Marketing Category: BLA
• Application Number: BLA125154
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: ML
• Marketing Start Date: 2006-10-17
• Inactivation Date: 2019-10-21

Drug Details

Active Ingredients

Ingredient	Strength
ALBUMIN (HUMAN)	50 g/1000mL

OpenFDA Data

• SPL SET ID: a912d27c-00cb-2ed0-effe-2d88d1f2ca67
• Manufacturer:
  • Octapharma Pharmazeutika Produktionsgesellschaft m.b.H.
• UNII:
  • ZIF514RVZR
• RxNorm Concept Unique ID - RxCUI:
  • 1741423
  • 1741420
  • 1741410
• Pharm Class PE:
  • Increased Oncotic Pressure [PE]
  • Increased Intravascular Volume [PE]
• PHarm Class EPC:
  • Human Serum Albumin [EPC]
• NUI Code:
  • N0000010288
  • N0000009361
  • N0000169504
  • N0000009457
  • N0000184174

Pharmacological Class

• Human Serum Albumin [EPC]
• Increased Intravascular Volume [PE]
• Increased Oncotic Pressure [PE]
• Osmotic Activity [MoA]
• Serum Albumin [Chemical/Ingredient]

NDC Crossover Matching brand name "Albumin (Human)" or generic name "Albumin Human"

NDC	Brand Name	Generic Name
68982-633	Albumin (Human)	Albumin (Human)
68982-643	Albumin (Human)	Albumin (Human)
68982-623	Albumin (Human)	Albumin (Human)
67467-633	Albumin (Human)	Albumin (Human)
67467-643	Albumin (Human)	Albumin (Human)
67467-623	Albumin (Human)	Albumin (Human)
0053-7680	Albuminar-25	Albumin (Human)
0053-7670	Albuminar-5	Albumin (Human)
64208-2510	ALBUMINEX	Albumin Human
44206-251	AlbuRx	ALBUMIN (HUMAN)
44206-310	ALBURX	ALBUMIN (HUMAN)
0944-0493	FLEXBUMIN	Albumin Human
0944-0495	Flexbumin	Albumin Human
61953-0001	HUMAN ALBUMIN GRIFOLS	ALBUMIN (HUMAN)
61953-0002	HUMAN ALBUMIN GRIFOLS	ALBUMIN (HUMAN)
13533-683	Plasbumin	Albumin (Human)
13533-684	Plasbumin	Albumin (Human)
13533-690	Plasbumin	Albumin (Human)
13533-691	Plasbumin	Albumin (Human)
13533-692	Plasbumin	Albumin (Human)