NDC Product Labeler Sun Pharmaceutical Industries Limited

Sun Pharmaceutical Industries Limited labeler's code is 54907. The labeler has 14 products that have an assigned National Drug Code.

NDC	Proprietary Name	Non-Proprietary Name	Dosage Form	Route Name	Product Type	Status
70095-017	Theophylline	Theophylline	Tablet, Extended Release	Oral	Human Prescription Drug	ACTIVE
70095-018	Theophylline	Theophylline	Tablet, Extended Release	Oral	Human Prescription Drug	ACTIVE
70095-019	Bisoprolol Fumarate	Bisoprolol Fumarate	Tablet, Film Coated	Oral	Human Prescription Drug	ACTIVE
70095-020	Bisoprolol Fumarate	Bisoprolol Fumarate	Tablet, Film Coated	Oral	Human Prescription Drug	ACTIVE
70095-024	Pantoprazole Sodium	Pantoprazole Sodium	Injection, Powder, Lyophilized, For Solution	Intravenous	Human Prescription Drug	ACTIVE
70095-025	Azithromycin Monohydrate	Azithromycin Monohydrate	Injection, Powder, Lyophilized, For Solution	Intravenous	Human Prescription Drug	ACTIVE
70095-026	Desmopressin Acetate	Desmopressin Acetate	Injection, Solution	Intravenous; Subcutaneous	Human Prescription Drug	ACTIVE
70095-031	Desmopressin Acetate	Desmopressin Acetate	Injection, Solution	Intravenous; Subcutaneous	Human Prescription Drug	ACTIVE
70095-040	Deflazacort	Deflazacort	Tablet	Oral	Human Prescription Drug	ACTIVE
70095-041	Deflazacort	Deflazacort	Tablet	Oral	Human Prescription Drug	ACTIVE
70095-042	Deflazacort	Deflazacort	Tablet	Oral	Human Prescription Drug	ACTIVE
70095-043	Deflazacort	Deflazacort	Tablet	Oral	Human Prescription Drug	ACTIVE
70095-050	Sodium Bicarbonate	Sodium Bicarbonate	Injection, Solution	Intravenous	Human Prescription Drug	ACTIVE
70095-080	Eribulin Mesylate	Eribulin Mesylate	Injection	Intravenous	Human Prescription Drug	ACTIVE