Calcium Carbonate
- Product NDC
- 0054-3117
- 11-digit product format
- 000543117
- Labeler code
- 0054
- Product ID
- 0054-3117_8c0aefee-0ab5-4a1b-9a5f-0107ab3e0681
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Calcium Carbonate
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Application
- part331
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2004-11-18
- Marketing end
- 2024-05-31
- Substance
- CALCIUM CARBONATE
- Active strength
- 1250 mg/5mL
- Pharmacologic classes
- Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE]
- 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 |
|---|
| 0054-3117-63 | 00054311763 | 500 mL in 1 BOTTLE (0054-3117-63) | 500 ml | 2004-11-18 | 2024-05-31 | No | No | Current |