NDC 17089-378

GUNA-INF GAMMA

Interferon Gamma-1b

GUNA-INF GAMMA is a Oral Solution/ Drops in the Human Otc Drug category. It is labeled and distributed by Guna Spa. The primary component is Interferon Gamma-1b.

• Product ID: 17089-378_7dd65a43-607e-1f16-e053-2a91aa0a466d
• NDC: 17089-378
• Product Type: Human Otc Drug
• Proprietary Name: GUNA-INF GAMMA
• Generic Name: Interferon Gamma-1b
• Dosage Form: Solution/ Drops
• Route of Administration: ORAL
• Marketing Start Date: 2008-06-17
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Guna spa
• Substance Name: INTERFERON GAMMA-1B
• Active Ingredient Strength: 4 [hp_C]/30mL
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 17089-378-18

1 BOTTLE, DROPPER in 1 BOX (17089-378-18) > 30 mL in 1 BOTTLE, DROPPER

• Marketing Start Date: 2008-06-17
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 17089-378-18 [17089037818]

GUNA-INF GAMMA SOLUTION/ DROPS

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2008-06-17
• Inactivation Date: 2020-01-31
• Reactivation Date: 2020-03-13

Drug Details

Active Ingredients

Ingredient	Strength
INTERFERON GAMMA-1B	4 [hp_C]/30mL

OpenFDA Data

• SPL SET ID: a09a33a1-5c7c-493d-abc7-907edd8e97ca
• Manufacturer:
  • Guna spa
• UNII:
  • 21K6M2I7AG
• UPC Code:
  • 0317089378181

NDC Crossover Matching brand name "GUNA-INF GAMMA" or generic name "Interferon Gamma-1b"

NDC	Brand Name	Generic Name
17089-378	GUNA-INF GAMMA	INTERFERON GAMMA-1B
75987-111	ACTIMMUNE	Interferon gamma-1b