Lithium Carbonate
- Product NDC
- 72789-172
- 11-digit product format
- 727890172
- Labeler code
- 72789
- Product ID
- 72789-172_40a77777-638f-c92e-e063-6394a90ae6d4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lithium Carbonate
- Dosage form
- CAPSULE, GELATIN COATED
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- NDA017812
- Marketing category
- NDA
- Marketing start
- 1987-01-28
- Substance
- LITHIUM CARBONATE
- Active strength
- 600 mg/1
- Pharmacologic classes
- Mood Stabilizer [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Lithium Carbonate
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| LITHIUM CARBONATE | 600 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 2BMD2GNA4V |
| Rxcui | 197893 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72789-172-01 | Lithium Carbonate | 100 in 1 BOTTLE, PLASTIC | CAPSULE, GELATIN COATED | 100 | | 30 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72789-172 | LITHIUM CARBONATE CAPSULE, GELATIN COATED [PD-RX PHARMACEUTICALS, INC.] | 29 | Current NDC, Legacy NDC, 1 package rows | 20241011_16ebe1f9-501d-468b-a37d-f6a46f8f32d1.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 |
|---|
| 72789-172-01 | 72789017201 | 100 CAPSULE, GELATIN COATED in 1 BOTTLE, PLASTIC (72789-172-01) | 2021-03-12 | 0000-00-00 | No | No | Current |