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SULFACETAMIDE SODIUM - 16590-209-15 - (SULFACETAMIDE SODIUM)

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Drug Information of SULFACETAMIDE SODIUM

Product NDC: 16590-209
Proprietary Name: SULFACETAMIDE SODIUM
Non Proprietary Name: SULFACETAMIDE SODIUM
Active Ingredient(s): 100    mg/mL & nbsp;   SULFACETAMIDE SODIUM
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of SULFACETAMIDE SODIUM

Product NDC: 16590-209
Labeler Name: STAT RX USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089560
Marketing Category: ANDA
Start Marketing Date: 19881018

Package Information of SULFACETAMIDE SODIUM

Package NDC: 16590-209-15
Package Description: 15 mL in 1 BOTTLE, PLASTIC (16590-209-15)

NDC Information of SULFACETAMIDE SODIUM

NDC Code 16590-209-15
Proprietary Name SULFACETAMIDE SODIUM
Package Description 15 mL in 1 BOTTLE, PLASTIC (16590-209-15)
Product NDC 16590-209
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name SULFACETAMIDE SODIUM
Dosage Form Name SOLUTION/ DROPS
Route Name OPHTHALMIC
Start Marketing Date 19881018
Marketing Category Name ANDA
Labeler Name STAT RX USA LLC
Substance Name SULFACETAMIDE SODIUM
Strength Number 100
Strength Unit mg/mL
Pharmaceutical Classes Sulfonamide Antibacterial [EPC],Sulfonamides [Chemical/Ingredient]

Complete Information of SULFACETAMIDE SODIUM


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