Calcium Acetate
- Product NDC
- 17856-0377
- 11-digit product format
- 178560377
- Labeler code
- 17856
- Product ID
- 17856-0377_c9bef39c-337b-4e5c-b225-43fb689eb50e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Calcium Acetate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Atlantic Biologicals Corps
- Application
- ANDA203135
- Marketing category
- ANDA
- Marketing start
- 2014-02-03
- Marketing end
- 0000-00-00
- Substance
- CALCIUM ACETATE
- Active strength
- 667 mg/1
- Pharmacologic classes
- Blood Coagulation Factor [EPC],Increased Coagulation Factor Activity [PE],Calcium [CS],Cations, Divalent [CS]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 17856-0377-2 | Calcium Acetate | 50 in 1 CASE | CAPSULE | 50 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 17856-0377 | CALCIUM ACETATE CAPSULE [ATLANTIC BIOLOGICALS CORPS] | 3 | Legacy NDC, 1 package rows | 20160527_fb8768f1-d2db-42bf-ac28-77a981afa798.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 17856-0377-2 | 17856037702 | 50 in 1 CASE | Historical |