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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 202885
Company: HERITAGE PHARMS INC

Products on ANDA 202885

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	TE Code	RLD	RS
CALCIUM ACETATE	CALCIUM ACETATE	667MG	TABLET;ORAL	Prescription	AB	No	No

Approval Date(s) and History, Letters, Labels, Reviews for ANDA 202885

Original Approvals or Tentative Approvals

Action Date	Submission	Action Type	Submission Classification	Review Priority; Orphan Status	Letters, Reviews, Labels, Patient Package Insert	Notes	Url
01/22/2015	ORIG-1	Approval				Label is not available on this site.

Therapeutic Equivalents for ANDA 202885

CALCIUM ACETATE

TABLET;ORAL; 667MG
TE Code = AB

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	RLD	TE Code	Application No.	Company
CALCIUM ACETATE	CALCIUM ACETATE	667MG	TABLET;ORAL	Prescription	No	AB	202420	CHARTWELL MOLECULAR
CALCIUM ACETATE	CALCIUM ACETATE	667MG	TABLET;ORAL	Prescription	No	AB	202885	HERITAGE PHARMS INC

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