Calcium Acetate
- Product NDC
- 70518-2372
- 11-digit product format
- 705182372
- Labeler code
- 70518
- Product ID
- 70518-2372_ef17805e-07ea-0c49-e053-2a95a90a16b6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Calcium Acetate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- NDA021160
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2019-10-21
- 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 |
|---|
| 70518-2372-0 | 70518237200 | 30 CAPSULE in 1 BLISTER PACK (70518-2372-0) | 30 capsule | 2019-10-21 | 0000-00-00 | No | No | Current |