Calcium Acetate
- Product NDC
- 0781-2672
- 11-digit product format
- 007812672
- Labeler code
- 0781
- Product ID
- 0781-2672_ecf8e9e7-faa4-431b-e053-2995a90a3e36
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Calcium Acetate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Sandoz Inc
- Application
- NDA021160
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2012-03-14
- Marketing end
- 0000-00-00
- Substance
- CALCIUM ACETATE
- Active strength
- 667 mg/1
- Pharmacologic classes
- Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0781-2672-02 | 00781267202 | 200 CAPSULE in 1 BOTTLE (0781-2672-02) | 200 capsule | 2012-03-14 | 0000-00-00 | No | No | Current |