lithium carbonate
- Product NDC
- 63629-1916
- 11-digit product format
- 636291916
- Labeler code
- 63629
- Product ID
- 63629-1916_a3dd12eb-9583-418a-ac98-bd04be426602
- 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 |
|---|
| 63629-1916-1 | 63629191601 | 100 CAPSULE in 1 BOTTLE (63629-1916-1) | 100 capsule | 2009-12-15 | 0000-00-00 | No | No | Current |