CALCIUM ACETATE
- Product NDC
- 0904-6668
- 11-digit product format
- 009046668
- Labeler code
- 0904
- Product ID
- 0904-6668_41efa69f-96f2-41bd-9f5e-f3da4ece493c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- calcium acetate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA202315
- Marketing category
- ANDA
- Marketing start
- 2015-07-07
- 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
- 2022-12-31
- 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 |
|---|
| 0904-6668-25 | 00904666825 | 200 CAPSULE in 1 BOTTLE (0904-6668-25) | 200 capsule | 2015-07-07 | 0000-00-00 | No | No | Current |