Calcium Acetate
- Product NDC
- 40051-049
- 11-digit product format
- 400510049
- Labeler code
- 40051
- Product ID
- 40051-049_96051d8c-ecb1-538e-e053-2995a90ab08d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Calcium Acetate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Lotus Pharmaceutical Co., Ltd. Nantou Plant
- Application
- ANDA203298
- Marketing category
- ANDA
- Marketing start
- 2016-09-01
- 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
- 2020-12-31
- 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 |
|---|
| 40051-049-01 | 40051004901 | 200 CAPSULE in 1 BOTTLE, PLASTIC (40051-049-01) | 200 capsule | 2016-09-01 | 0000-00-00 | No | No | Current |