Lithium Carbonate
- Product NDC
- 70518-2086
- 11-digit product format
- 705182086
- Labeler code
- 70518
- Product ID
- 70518-2086_499db2fe-4805-e2f7-e063-6394a90ab068
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lithium Carbonate
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA205663
- Marketing category
- ANDA
- Marketing start
- 2019-05-16
- Substance
- LITHIUM CARBONATE
- Active strength
- 450 mg/1
- Pharmacologic classes
- Mood Stabilizer [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Lithium Carbonate
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| LITHIUM CARBONATE | 450 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 2BMD2GNA4V |
| Rxcui | 197892 |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70518-2086-0 | Lithium Carbonate | 30 in 1 BLISTER PACK | TABLET, EXTENDED RELEASE | 30 | | 12 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-2086 | LITHIUM CARBONATE TABLET, EXTENDED RELEASE [REMEDYREPACK INC.] | 9 | Current NDC, Legacy NDC, 1 package rows | 20250306_db3dc13f-d532-4fcd-a235-c9efab9e6bd7.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2086-0 | 70518208600 | 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-2086-0) | 2019-05-16 | 0000-00-00 | No | No | Current |