Lithium Carbonate
- Product NDC
- 70518-4589
- 11-digit product format
- 705184589
- Labeler code
- 70518
- Product ID
- 70518-4589_4d740916-d8f8-0331-e063-6394a90a894a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lithium Carbonate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA091616
- Marketing category
- ANDA
- Marketing start
- 2026-03-20
- Substance
- LITHIUM CARBONATE
- Active strength
- 450 mg/1
- Pharmacologic classes
- Mood Stabilizer [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 2BMD2GNA4V | LITHIUM CARBONATE | 554-13-2 | LITHIUM CARBONATE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 70518-4589-0 | 70518458900 | 30 TABLET in 1 BLISTER PACK (70518-4589-0) | 30 tablet | 2026-03-20 | No | No | Historical |