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GUNA-INF ALPHA
GUNA-INF ALPHA - 17089-456-18 - (INTERFERON ALFA-2A)
Drug Information of GUNA-INF ALPHA
| Product NDC: | 17089-456 |
| Proprietary Name: | GUNA-INF ALPHA |
| Non Proprietary Name: | INTERFERON ALFA-2A |
| Active Ingredient(s): | 4 [hp_C]/30mL & nbsp; INTERFERON ALFA-2A |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of GUNA-INF ALPHA
| Product NDC: | 17089-456 |
| Labeler Name: | Guna spa |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20110216 |
Package Information of GUNA-INF ALPHA
| Package NDC: | 17089-456-18 |
| Package Description: | 1 BOTTLE, DROPPER in 1 BOX (17089-456-18) > 30 mL in 1 BOTTLE, DROPPER |
NDC Information of GUNA-INF ALPHA
| NDC Code | 17089-456-18 |
| Proprietary Name | GUNA-INF ALPHA |
| Package Description | 1 BOTTLE, DROPPER in 1 BOX (17089-456-18) > 30 mL in 1 BOTTLE, DROPPER |
| Product NDC | 17089-456 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | INTERFERON ALFA-2A |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | ORAL |
| Start Marketing Date | 20110216 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Guna spa |
| Substance Name | INTERFERON ALFA-2A |
| Strength Number | 4 |
| Strength Unit | [hp_C]/30mL |
| Pharmaceutical Classes |
