Calcium Acetate
- Product NDC
- 0615-8090
- 11-digit product format
- 006158090
- Labeler code
- 0615
- Product ID
- 0615-8090_f27dd452-e15a-4d1e-bc50-fcb572070479
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Calcium Acetate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, Inc dba Vangard Labs
- Application
- ANDA201658
- Marketing category
- ANDA
- Marketing start
- 2014-10-08
- Marketing end
- 2021-10-31
- 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
- 0000-00-00
- 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 |
|---|
| 0615-8090-30 | 00615809030 | 6 BLISTER PACK in 1 BOX, UNIT-DOSE (0615-8090-30) > 5 CAPSULE in 1 BLISTER PACK | 6 blister pack | 2017-07-11 | 2021-10-31 | No | No | Current |
| 0615-8090-39 | 00615809039 | 30 CAPSULE in 1 BLISTER PACK (0615-8090-39) | 30 capsule | 2017-07-13 | 2021-10-31 | No | No | Current |