Chlorthalidone
- Product NDC
- 60290-004
- 11-digit product format
- 602900004
- Labeler code
- 60290
- Product ID
- 60290-004_50581ec8-6ab6-82ae-e063-6294a90af70f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlorthalidone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Umedica Laboratories USA Inc.
- Application
- ANDA207222
- Marketing category
- ANDA
- Marketing start
- 2026-02-15
- Substance
- CHLORTHALIDONE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Increased Diuresis [PE], Thiazide-like Diuretic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Chlorthalidone
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CHLORTHALIDONE | 25 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | Q0MQD1073Q |
| Rxcui | 197499, 197500 |
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 |
|---|
| 60290-004-01 | Chlorthalidone | 100 in 1 BOTTLE | TABLET | 100 | | 3 |
| 60290-004-02 | Chlorthalidone | 1000 in 1 BOTTLE | TABLET | 1000 | | 3 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 60290-004-01 | 60290000401 | 100 TABLET in 1 BOTTLE (60290-004-01) | 100 tablet | 2026-02-15 | No | No | Historical |
| 60290-004-02 | 60290000402 | 1000 TABLET in 1 BOTTLE (60290-004-02) | 1000 tablet | 2026-02-15 | No | No | Historical |