Lithium Carbonate
- Product NDC
- 71205-238
- 11-digit product format
- 712050238
- Labeler code
- 71205
- Product ID
- 71205-238_0745a72f-4b61-4664-a3ef-30b7e51d4b7b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lithium Carbonate Extended-Release Tablet
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- NDA018027
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2016-12-21
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71205-238 | LITHIUM CARBONATE (LITHIUM CARBONATE EXTENDED-RELEASE TABLET) TABLET, FILM COATED, EXTENDED RELEASE [PROFICIENT RX LP] | 2 | Legacy NDC | 20191012_69abce83-543a-44fb-891f-1d271e7cf19a.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71205-238-30 | 71205023830 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-238-30) | 2019-03-01 | 0000-00-00 | No | No | Current |
| 71205-238-60 | 71205023860 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-238-60) | 2019-03-01 | 0000-00-00 | No | No | Current |
| 71205-238-90 | 71205023890 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-238-90) | 2019-03-01 | 0000-00-00 | No | No | Current |