GAMMA -12

Product NDC
17089-405
11-digit product format
170890405
Labeler code
17089
Product ID
17089-405_ed853c61-ca74-4c3d-e053-2995a90aecb9
Type
HUMAN OTC DRUG
Nonproprietary name
INTERLEUKIN-12 HUMAN RECOMBINANT - INTERFERON GAMMA-1B -
Dosage form
SOLUTION/ DROPS
Route
ORAL
Labeler
Guna spa
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2010-04-29
Substance
INTERFERON GAMMA-1B; INTERLEUKIN-12 HUMAN RECOMBINANT
Active strength
4; 4 [hp_C]/30mL; [hp_C]/30mL
Pharmacologic classes
Interferon gamma [EPC], Interferon-gamma [CS]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
GAMMA -12
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
INTERFERON GAMMA-1B4 [hp_C]/30mL
INTERLEUKIN-12 HUMAN RECOMBINANT4 [hp_C]/30mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii21K6M2I7AG, 02FXP10O2U

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
d45267e3-883a-4760-85b5-ebc565c21683Product name120150910

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
17089-405-18GAMMA -1230 mL in 1 BOTTLE, DROPPERSOLUTION/ DROPS305
17089-405-18GAMMA -121 in 1 BOXSOLUTION/ DROPS15

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
17089-405GAMMA -12 (INTERLEUKIN-12 HUMAN RECOMBINANT - INTERFERON GAMMA-1B -) SOLUTION/ DROPS [GUNA SPA]5Current NDC, Legacy NDC, 2 package rows20221116_c3366fcd-7d7a-4cf8-995c-798b6d2c9ad1.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
17089-405-18170890405181 BOTTLE, DROPPER in 1 BOX (17089-405-18) / 30 mL in 1 BOTTLE, DROPPER2011-03-310000-00-00NoNoCurrent