lithium carbonate
- Product NDC
- 63629-9190
- 11-digit product format
- 636299190
- Labeler code
- 63629
- Product ID
- 63629-9190_a0a74837-332d-4330-9783-76a3efe2b10e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lithium carbonate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA090702
- Marketing category
- ANDA
- Marketing start
- 2009-12-15
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-9190-1 | 63629919001 | 1000 CAPSULE in 1 BOTTLE (63629-9190-1) | 1000 capsule | 2022-08-03 | 0000-00-00 | No | No | Current |