Lithium Carbonate
- Product NDC
- 46708-303
- 11-digit product format
- 467080303
- Labeler code
- 46708
- Product ID
- 46708-303_f4a09dd5-000a-48d2-9681-d5bc360164f1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lithium Carbonate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Alembic Pharmaceuticals Limited
- Application
- ANDA079159
- Marketing category
- ANDA
- Marketing start
- 2016-12-27
- Substance
- LITHIUM CARBONATE
- Active strength
- 150 mg/1
- Pharmacologic classes
- Mood Stabilizer [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- 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 |
|---|
| 46708-303-30 | 46708030330 | 30 CAPSULE in 1 BOTTLE (46708-303-30) | 30 capsule | 2016-12-27 | No | No | Historical |
| 46708-303-31 | 46708030331 | 100 CAPSULE in 1 BOTTLE (46708-303-31) | 100 capsule | 2016-12-27 | No | No | Historical |
| 46708-303-71 | 46708030371 | 500 CAPSULE in 1 BOTTLE (46708-303-71) | 500 capsule | 2016-12-27 | No | No | Historical |
| 46708-303-91 | 46708030391 | 1000 CAPSULE in 1 BOTTLE (46708-303-91) | 1000 capsule | 2016-12-27 | No | No | Historical |