Calcium Acetate
- Product NDC
- 71335-0621
- 11-digit product format
- 713350621
- Labeler code
- 71335
- Product ID
- 71335-0621_32547eae-be4d-4604-acb0-a7a6c4707b8b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Calcium Acetate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA201658
- Marketing category
- ANDA
- Marketing start
- 2014-10-08
- 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
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record