Calcium Acetate
- Product NDC
- 71335-1351
- 11-digit product format
- 713351351
- Labeler code
- 71335
- Product ID
- 71335-1351_20aeb36b-cb23-45f5-8316-01509e8ab627
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Calcium Acetate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- NDA021160
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2012-03-14
- Marketing end
- 0000-00-00
- Substance
- CALCIUM ACETATE
- Active strength
- 667 mg/1
- Pharmacologic classes
- Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 71335-1351-1 | 71335135101 | 30 CAPSULE in 1 BOTTLE (71335-1351-1) | 30 capsule | 2012-03-14 | 0000-00-00 | No | No | Current |
| 71335-1351-2 | 71335135102 | 90 CAPSULE in 1 BOTTLE (71335-1351-2) | 90 capsule | 2012-03-14 | 0000-00-00 | No | No | Current |
| 71335-1351-3 | 71335135103 | 200 CAPSULE in 1 BOTTLE (71335-1351-3) | 200 capsule | 2012-03-14 | 0000-00-00 | No | No | Current |
| 71335-1351-4 | 71335135104 | 28 CAPSULE in 1 BOTTLE (71335-1351-4) | 28 capsule | 2012-03-14 | 0000-00-00 | No | No | Current |