Lithium carbonate
- Product NDC
- 23155-293
- 11-digit product format
- 231550293
- Labeler code
- 23155
- Product ID
- 23155-293_6f564944-dbc5-4ca5-88b1-b8c9e9886d30
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lithium carbonate
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Heritage Pharmaceuticals Inc.
- Application
- ANDA205532
- Marketing category
- ANDA
- Marketing start
- 2013-03-30
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record