Calcium Acetate
- Product NDC
- 71335-0172
- 11-digit product format
- 713350172
- Labeler code
- 71335
- Product ID
- 71335-0172_759503b5-ef29-4a42-abea-601adcf03b0f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Calcium Acetate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077728
- Marketing category
- ANDA
- Marketing start
- 2008-02-26
- 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 |
|---|
| 71335-0172-1 | 71335017201 | 30 CAPSULE in 1 BOTTLE (71335-0172-1) | 30 capsule | 2021-12-27 | 0000-00-00 | No | No | Current |
| 71335-0172-2 | 71335017202 | 90 CAPSULE in 1 BOTTLE (71335-0172-2) | 90 capsule | 2021-12-27 | 0000-00-00 | No | No | Current |
| 71335-0172-3 | 71335017203 | 200 CAPSULE in 1 BOTTLE (71335-0172-3) | 200 capsule | 2021-12-27 | 0000-00-00 | No | No | Current |
| 71335-0172-4 | 71335017204 | 28 CAPSULE in 1 BOTTLE (71335-0172-4) | 28 capsule | 2021-12-27 | 0000-00-00 | No | No | Current |