Lithium Carbonate
- Product NDC
- 68151-0639
- 11-digit product format
- 681510639
- Labeler code
- 68151
- Product ID
- 68151-0639_dd6eb08e-888a-4be4-88d1-80c27f18a74f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lithium Carbonate
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Carilion Materials Management
- Application
- ANDA076832
- Marketing category
- ANDA
- Marketing start
- 2004-10-28
- Marketing end
- 0000-00-00
- Substance
- LITHIUM CARBONATE
- Active strength
- 300 mg/1
- Pharmacologic classes
- Mood Stabilizer [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| b3053bb1-353b-4a0b-bca5-28fe7228957c | Product name | 2 | 20250124 |
| 8ce6e144-236f-b7be-f690-f06e0c8c6bd3 | Product name | 2 | 20170725 |
| f09af6ee-c6dd-d0ce-77ad-93508bcdaced | Product name | 4 | 20161205 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 68151-0639-2 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-e2f3-f424-e053-dadaa90a57ce | Lithium Carbonate Extended-release Tablets USP, 300 mg |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 68151-0639-2 | Lithium Carbonate | 1 in 1 PACKAGE | TABLET, EXTENDED RELEASE | 1 | 4 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| LITHIUM CARBONATE | ACTIVE INGREDIENT | 2BMD2GNA4V | LITHIUM CARBONATE TABLET, EXTENDED RELEASE [CARILION MATERIALS MANAGEMENT] | 2 | |
| LITHIUM CATION | ACTIVE MOIETY | 8H8Z5UER66 | LITHIUM CARBONATE TABLET, EXTENDED RELEASE [CARILION MATERIALS MANAGEMENT] | 2 | |
| CALCIUM STEARATE | INACTIVE INGREDIENT | 776XM7047L | LITHIUM CARBONATE TABLET, EXTENDED RELEASE [CARILION MATERIALS MANAGEMENT] | 2 | |
| POVIDONES | INACTIVE INGREDIENT | FZ989GH94E | LITHIUM CARBONATE TABLET, EXTENDED RELEASE [CARILION MATERIALS MANAGEMENT] | 2 | |
| SODIUM CHLORIDE | INACTIVE INGREDIENT | 451W47IQ8X | LITHIUM CARBONATE TABLET, EXTENDED RELEASE [CARILION MATERIALS MANAGEMENT] | 2 | |
| SODIUM LAURYL SULFATE | INACTIVE INGREDIENT | 368GB5141J | LITHIUM CARBONATE TABLET, EXTENDED RELEASE [CARILION MATERIALS MANAGEMENT] | 2 | |
| SORBITOL | INACTIVE INGREDIENT | 506T60A25R | LITHIUM CARBONATE TABLET, EXTENDED RELEASE [CARILION MATERIALS MANAGEMENT] | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 68151-0639 | LITHIUM CARBONATE TABLET, EXTENDED RELEASE [CARILION MATERIALS MANAGEMENT] | 4 | Legacy NDC, 1 package rows | 20170706_7f3aa4f5-908a-44e7-8113-b64f91dc86e7.zip |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 197891 | lithium carbonate 300 MG Extended Release Oral Tablet | PSN | 7f3aa4f5-908a-44e7-8113-b64f91dc86e7 | 4 |
| 197891 | lithium carbonate 300 MG Extended Release Oral Tablet | SCD | 7f3aa4f5-908a-44e7-8113-b64f91dc86e7 | 4 |
| 197891 | LiCO3 300 MG Extended Release Oral Tablet | SY | 7f3aa4f5-908a-44e7-8113-b64f91dc86e7 | 4 |
Packages#
| Package NDC | 11-digit format | Description | Status |
|---|---|---|---|
| 68151-0639-2 | 68151063902 | 1 in 1 PACKAGE | Historical |