Lithium Carbonate
- Product NDC
- 0615-2304
- 11-digit product format
- 006152304
- Labeler code
- 0615
- Product ID
- 0615-2304_332d9499-f831-4d29-9270-43370119d957
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lithium Carbonate
- Dosage form
- CAPSULE, GELATIN COATED
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, Inc dba Vangard Labs
- Application
- NDA017812
- Marketing category
- NDA
- Marketing start
- 1987-01-28
- Marketing end
- 0000-00-00
- Substance
- LITHIUM CARBONATE
- Active strength
- 150 mg/1
- Pharmacologic classes
- Mood Stabilizer [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#