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Streptomycin
Streptomycin - 39822-0706-2 - (Streptomycin)
Drug Information of Streptomycin
| Product NDC: | 39822-0706 |
| Proprietary Name: | Streptomycin |
| Non Proprietary Name: | Streptomycin |
| Active Ingredient(s): | 1 g/1 & nbsp; Streptomycin |
| Administration Route(s): | INTRAMUSCULAR |
| Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Streptomycin
| Product NDC: | 39822-0706 |
| Labeler Name: | X-GEN Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA064210 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19980630 |
Package Information of Streptomycin
| Package NDC: | 39822-0706-2 |
| Package Description: | 10 VIAL in 1 BOX (39822-0706-2) > 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (39822-0706-1) |
NDC Information of Streptomycin
| NDC Code | 39822-0706-2 |
| Proprietary Name | Streptomycin |
| Package Description | 10 VIAL in 1 BOX (39822-0706-2) > 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (39822-0706-1) |
| Product NDC | 39822-0706 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Streptomycin |
| Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route Name | INTRAMUSCULAR |
| Start Marketing Date | 19980630 |
| Marketing Category Name | ANDA |
| Labeler Name | X-GEN Pharmaceuticals, Inc. |
| Substance Name | STREPTOMYCIN SULFATE |
| Strength Number | 1 |
| Strength Unit | g/1 |
| Pharmaceutical Classes | Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient],Antimycobacterial [EPC] |
