Calcium Acetate
- Product NDC
- 62135-192
- 11-digit product format
- 621350192
- Labeler code
- 62135
- Product ID
- 62135-192_2471197e-c8a7-c3c7-e063-6394a90a16d7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Calcium Acetate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Chartwell RX LLC
- Application
- ANDA202420
- Marketing category
- ANDA
- Marketing start
- 2019-07-01
- 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
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Calcium Acetate
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CALCIUM ACETATE | 667 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | Y882YXF34X |
| Rxcui | 197433 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 62135-192-22 | Calcium Acetate | 200 in 1 BOTTLE | TABLET | 200 | | 8 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 62135-192 | CALCIUM ACETATE TABLET [CHARTWELL RX LLC] | 8 | Current NDC, Legacy NDC, 1 package rows | 20241016_9584350a-b6ad-45ae-b1c5-c8ca8f471c03.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 |
|---|
| 62135-192-22 | 62135019222 | 200 TABLET in 1 BOTTLE (62135-192-22) | 200 tablet | 2019-07-01 | 0000-00-00 | No | No | Current |