Lithium Carbonate
- Product NDC
- 50090-1722
- 11-digit product format
- 500901722
- Labeler code
- 50090
- Product ID
- 50090-1722_57c5a5ef-02ac-4785-b32e-b72a6b9aab93
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lithium Carbonate
- Dosage form
- CAPSULE, GELATIN COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- NDA017812
- Marketing category
- NDA
- Marketing start
- 1980-11-26
- Marketing end
- 0000-00-00
- Substance
- LITHIUM CARBONATE
- Active strength
- 300 mg/1
- Pharmacologic classes
- Mood Stabilizer [EPC]
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-1722-1 | 50090172201 | 90 CAPSULE, GELATIN COATED in 1 BOTTLE (50090-1722-1) | 2015-03-04 | 0000-00-00 | No | No | Current |