Calcium Acetate

Product NDC: 31722-393
11-digit product format: 317220393
Labeler code: 31722
Product ID: 31722-393_3af1f87c-2e11-47a7-8ace-719dafaac0be
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Calcium Acetate
Dosage form: TABLET
Route: ORAL
Labeler: Camber Pharmaceuticals, Inc.
Application: ANDA202420
Marketing category: ANDA
Marketing start: 2014-02-03
Marketing end: 0000-00-00
Substance: CALCIUM ACETATE
Active strength: 667 mg/1
Pharmacologic classes: Blood Coagulation Factor [EPC],Increased Coagulation Factor Activity [PE],Calcium [CS],Cations, Divalent [CS]
NDC exclude flag: E
Listing certified through: 2017-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
31722-393-60	2025-06-16	C162847	48780-1	9855e2a2-4e84-60a7-e053-dbdaa90a05bd	49453f19-f4f4-451c-a092-3ce084f9a429
31722-393-60	2019-11-27	C162847	48780-1	9855e2a2-4e84-60a7-e053-dbdaa90a05bd	49453f19-f4f4-451c-a092-3ce084f9a429

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
CALCIUM ACETATE	ACTIVE INGREDIENT	Y882YXF34X	CALCIUM ACETATE TABLET [CAMBER PHARMACEUTICALS, INC.]	1
CALCIUM CATION	ACTIVE MOIETY	2M83C4R6ZB	CALCIUM ACETATE TABLET [CAMBER PHARMACEUTICALS, INC.]	1
CROSPOVIDONE	INACTIVE INGREDIENT	68401960MK	CALCIUM ACETATE TABLET [CAMBER PHARMACEUTICALS, INC.]	1
POLYETHYLENE GLYCOL 8000	INACTIVE INGREDIENT	Q662QK8M3B	CALCIUM ACETATE TABLET [CAMBER PHARMACEUTICALS, INC.]	1
SODIUM LAURYL SULFATE	INACTIVE INGREDIENT	368GB5141J	CALCIUM ACETATE TABLET [CAMBER PHARMACEUTICALS, INC.]	1
SODIUM STEARYL FUMARATE	INACTIVE INGREDIENT	7CV7WJK4UI	CALCIUM ACETATE TABLET [CAMBER PHARMACEUTICALS, INC.]	1

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
31722-393	CALCIUM ACETATE TABLET [CAMBER PHARMACEUTICALS, INC.]	1	Legacy NDC	20140203_49453f19-f4f4-451c-a092-3ce084f9a429.zip