Calcium Acetate
- Product NDC
- 51293-825
- 11-digit product format
- 512930825
- Labeler code
- 51293
- Product ID
- 51293-825_a31cdbdf-ce20-4a53-aa25-9d8c81f567bd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Calcium Acetate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- ECI Pharmaceuticals, LLC
- Application
- ANDA203298
- Marketing category
- ANDA
- Marketing start
- 2017-02-25
- 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
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51293-825 | CALCIUM ACETATE CAPSULE [ECI PHARMACEUTICALS, LLC] | 3 | Legacy NDC | 20190701_3fe28f73-87ee-4ac1-9356-45c8760b20c7.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51293-825-02 | 51293082502 | 200 CAPSULE in 1 BOTTLE (51293-825-02) | 200 capsule | 2017-02-25 | 0000-00-00 | No | No | Current |