Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 215911
Company: LUPIN

Products on ANDA 215911

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	TE Code	RLD	RS
CALCIUM;MAGNESIUM;POTASSIUM;SODIUM OXYBATES	CALCIUM;MAGNESIUM;POTASSIUM;SODIUM OXYBATES	0.5G/ML	SOLUTION;ORAL	None (Tentative Approval)	None	No	No

Approval Date(s) and History, Letters, Labels, Reviews for ANDA 215911

Original Approvals or Tentative Approvals

Action Date	Submission	Action Type	Submission Classification	Review Priority; Orphan Status	Letters, Reviews, Labels, Patient Package Insert	Notes	Url
10/11/2023	ORIG-1	Tentative Approval		STANDARD	Letter (PDF)	Label is not available on this site.	https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2023/215911Orig1s000TAltr.pdf