Calcium Acetate
- Product NDC
- 72789-422
- 11-digit product format
- 727890422
- Labeler code
- 72789
- Product ID
- 72789-422_4123b0e5-2fcd-88fb-e063-6294a90a05e7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Calcium Acetate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA217205
- Marketing category
- ANDA
- Marketing start
- 2023-12-07
- Substance
- CALCIUM ACETATE
- Active strength
- 667 mg/1
- Pharmacologic classes
- Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| Y882YXF34X | CALCIUM ACETATE | 62-54-4 | CALCIUM ACETATE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72789-422-97 | 72789042297 | 200 CAPSULE in 1 BOTTLE, PLASTIC (72789-422-97) | 200 capsule | 2024-07-16 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Calcium Acetate | PD-Rx Pharmaceuticals, Inc. | 2025-10-14 | HUMAN PRESCRIPTION DRUG LABEL | 3 |
| Calcium Acetate | PD-Rx Pharmaceuticals, Inc. | 2024-07-16 | HUMAN PRESCRIPTION DRUG LABEL | 2 |