Calcium Acetate
- Product NDC
- 0615-2303
- 11-digit product format
- 006152303
- Labeler code
- 0615
- Product ID
- 0615-2303_938c3471-0c2e-43c2-88ba-ff5eb2e38fc3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Calcium Acetate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, Inc dba Vangard Labs
- Application
- ANDA077728
- Marketing category
- ANDA
- Marketing start
- 2008-02-26
- 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#