Lithium Carbonate
- Product NDC
- 58118-0545
- 11-digit product format
- 581180545
- Labeler code
- 58118
- Product ID
- 58118-0545_b02607c9-504d-b0d0-e053-2a95a90a7dc0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lithium Carbonate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Clinical Solutions Wholesale
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 58118-0545 | LITHIUM CARBONATE CAPSULE [CLINICAL SOLUTIONS WHOLESALE] | 10 | Legacy NDC | 20200926_3ec62ecc-677d-4f61-88a3-1bd9d9108fd5.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 58118-0545-8 | 58118054508 | 30 CAPSULE in 1 BLISTER PACK (58118-0545-8) | 30 capsule | 2009-12-15 | 0000-00-00 | No | No | Current |