Lithium Carbonate
- Product NDC
- 50090-2993
- 11-digit product format
- 500902993
- Labeler code
- 50090
- Product ID
- 50090-2993_66058448-6a5d-4645-89ce-c774c28ff93b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lithium Carbonate
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA076691
- Marketing category
- ANDA
- Marketing start
- 2004-01-05
- Marketing end
- 0000-00-00
- Substance
- LITHIUM CARBONATE
- Active strength
- 450 mg/1
- Pharmacologic classes
- Mood Stabilizer [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#