Calcium Acetate
- Product NDC
- 42291-189
- 11-digit product format
- 422910189
- Labeler code
- 42291
- Product ID
- 42291-189_9c5c3dc2-48d8-7e0b-e053-2995a90a5711
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Calcium Acetate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- AvKARE, Inc.
- Application
- ANDA201658
- Marketing category
- ANDA
- Marketing start
- 2016-06-15
- 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
- 2021-12-31
- 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 |
|---|
| 42291-189-20 | 42291018920 | 200 CAPSULE in 1 BOTTLE (42291-189-20) | 200 capsule | 2016-06-15 | 0000-00-00 | No | No | Current |