Calcium Acetate
- Product NDC
- 49230-644
- 11-digit product format
- 492300644
- Labeler code
- 49230
- Product ID
- 49230-644_bd21ca87-90ce-2b1b-e053-2995a90ab3ea
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Calcium Acetate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Fresenius Medical Care North America
- Application
- NDA021160
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2019-06-01
- Marketing end
- 2024-04-30
- Substance
- CALCIUM ACETATE
- Active strength
- 667 mg/667mg
- Pharmacologic classes
- Blood Coagulation Factor [EPC],Increased Coagulation Factor Activity [PE],Calcium [CS],Cations, Divalent [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 49230-644-41 | 49230064441 | 200 mg in 1 BOTTLE (49230-644-41) | 200 mg | 2019-06-01 | 2024-04-30 | No | No | Current |