Calcium Acetate
- Product NDC
- 68022-0119
- 11-digit product format
- 680220119
- Labeler code
- 68022
- Product ID
- 68022-0119_e587583d-d393-a292-e053-2995a90a17cb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Calcium Acetate Capsules 667 mg
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Suven Pharmaceuticals Limited
- Application
- ANDA211038
- Marketing category
- ANDA
- Marketing start
- 2020-01-10
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68022-0119 | CALCIUM ACETATE (CALCIUM ACETATE CAPSULES 667 MG) CAPSULE [SUVEN PHARMACEUTICALS LIMITED] | 10 | Legacy NDC | 20240110_78d66474-09e9-72a8-e053-2991aa0a76ec.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68022-0119-1 | 68022011901 | 1 CAPSULE in 1 BOTTLE, PLASTIC (68022-0119-1) | 1 capsule | 2020-01-10 | 0000-00-00 | No | No | Current |