lithium carbonate
- Product NDC
- 70518-0437
- 11-digit product format
- 705180437
- Labeler code
- 70518
- Product ID
- 70518-0437_e194dd4c-0746-2534-e053-2995a90af6ac
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lithium carbonate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA090702
- Marketing category
- ANDA
- Marketing start
- 2017-04-19
- 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 |
|---|
| 70518-0437-0 | 70518043700 | 30 CAPSULE in 1 BLISTER PACK (70518-0437-0) | 30 capsule | 2017-04-19 | 0000-00-00 | No | No | Current |
| 70518-0437-1 | 70518043701 | 100 POUCH in 1 BOX (70518-0437-1) > 1 CAPSULE in 1 POUCH (70518-0437-2) | 100 pouch | 2020-07-09 | 0000-00-00 | No | No | Current |