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Streptomycin

NDC 39822-0706 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Labeler / ManufacturerXGen Pharmaceuticals DJB, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA064210
Dosage form / routeINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAMUSCULAR
Active ingredientsSTREPTOMYCIN SULFATE (1 g/1)
Marketing started19980630
Package count1

External sources

Source: openFDA. Public-domain (CC0).