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GAMMA -12
GAMMA -12 - 17089-405-18 - (INTERLEUKIN-12 HUMAN RECOMBINANT - INTERFERON GAMMA-1B -)
Drug Information of GAMMA -12
| Product NDC: | 17089-405 |
| Proprietary Name: | GAMMA -12 |
| Non Proprietary Name: | INTERLEUKIN-12 HUMAN RECOMBINANT - INTERFERON GAMMA-1B - |
| Active Ingredient(s): | 4; 4 [hp_C]/30mL; [hp_C]/30mL & nbsp; INTERLEUKIN-12 HUMAN RECOMBINANT - INTERFERON GAMMA-1B - |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of GAMMA -12
| Product NDC: | 17089-405 |
| Labeler Name: | Guna spa |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20100429 |
Package Information of GAMMA -12
| Package NDC: | 17089-405-18 |
| Package Description: | 1 BOTTLE, DROPPER in 1 BOX (17089-405-18) > 30 mL in 1 BOTTLE, DROPPER |
NDC Information of GAMMA -12
| NDC Code | 17089-405-18 |
| Proprietary Name | GAMMA -12 |
| Package Description | 1 BOTTLE, DROPPER in 1 BOX (17089-405-18) > 30 mL in 1 BOTTLE, DROPPER |
| Product NDC | 17089-405 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | INTERLEUKIN-12 HUMAN RECOMBINANT - INTERFERON GAMMA-1B - |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | ORAL |
| Start Marketing Date | 20100429 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Guna spa |
| Substance Name | INTERFERON GAMMA-1B; INTERLEUKIN-12 HUMAN RECOMBINANT |
| Strength Number | 4; 4 |
| Strength Unit | [hp_C]/30mL; [hp_C]/30mL |
| Pharmaceutical Classes |
