CHLORTHALIDONE
- Product NDC
- 64980-304
- 11-digit product format
- 649800304
- Labeler code
- 64980
- Product ID
- 64980-304_94ef7a73-3872-4d19-bdde-881862337783
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CHLORTHALIDONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Rising Pharma Holdings, Inc.
- Application
- ANDA206904
- Marketing category
- ANDA
- Marketing start
- 2017-05-17
- Marketing end
- 2027-01-31
- Substance
- CHLORTHALIDONE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Increased Diuresis [PE], Thiazide-like Diuretic [EPC]
- NDC exclude flag
- No
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- CHLORTHALIDONE
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CHLORTHALIDONE | 50 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 |
|---|
| 64980-304-01 | CHLORTHALIDONE | 100 in 1 BOTTLE, PLASTIC | TABLET | 100 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 64980-304 | CHLORTHALIDONE TABLET [RISING PHARMA HOLDINGS, INC.] | 7 | Current NDC, Legacy NDC, 1 package rows | 20250503_f96b2d0b-a141-4efb-8ccc-c447dfc6024a.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 64980-304-01 | 64980030401 | 100 TABLET in 1 BOTTLE, PLASTIC (64980-304-01) | 100 tablet | 2017-05-17 | 2027-01-31 | No | No | Current |