Lithium Carbonate
- Product NDC
- 70518-0904
- 11-digit product format
- 705180904
- Labeler code
- 70518
- Product ID
- 70518-0904_e29a348d-2061-b97f-e053-2995a90ab972
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lithium carbonate
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA202288
- Marketing category
- ANDA
- Marketing start
- 2017-12-12
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-0904-0 | 70518090400 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-0904-0) | 2017-12-12 | 0000-00-00 | No | No | Current |