Calcium Acetate
- Product NDC
- 16571-813
- 11-digit product format
- 165710813
- Labeler code
- 16571
- Product ID
- 16571-813_3f799c80-1333-405d-ba78-4f1bc7e5d1ca
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Calcium Acetate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Rising Pharma Holdings, Inc.
- Application
- ANDA211038
- Marketing category
- ANDA
- Marketing start
- 2021-11-01
- 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
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Calcium Acetate
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CALCIUM ACETATE | 667 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | Y882YXF34X |
| Rxcui | 359296 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 16571-813-20 | Calcium Acetate | 200 in 1 BOTTLE, PLASTIC | CAPSULE | 200 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 16571-813 | CALCIUM ACETATE CAPSULE [RISING PHARMA HOLDINGS, INC.] | 4 | Current NDC, Legacy NDC, 1 package rows | 20241113_ce650ba5-fb42-e444-e053-2a95a90a075a.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 16571-813-20 | 16571081320 | 200 CAPSULE in 1 BOTTLE, PLASTIC (16571-813-20) | 200 capsule | 2021-11-01 | 0000-00-00 | No | No | Current |