CHLORTHALIDONE
- Product NDC
- 51655-477
- 11-digit product format
- 516550477
- Labeler code
- 51655
- Product ID
- 51655-477_490f4355-9be9-f19a-e063-6394a90af240
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CHLORTHALIDONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Northwind Health Company, LLC
- Application
- ANDA210742
- Marketing category
- ANDA
- Marketing start
- 2022-12-02
- Substance
- CHLORTHALIDONE
- Active strength
- 50 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 | 50 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | Q0MQD1073Q |
| Rxcui | 197500 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51655-477-52 | CHLORTHALIDONE | 30 in 1 BOTTLE, PLASTIC | TABLET | 30 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51655-477 | CHLORTHALIDONE TABLET [NORTHWIND PHARMACEUTICALS, LLC] | 1 | Current NDC, 1 package rows | 20230413_f309b5df-ce39-0d55-e053-2995a90a7878.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 51655-477-52 | 51655047752 | 30 TABLET in 1 BOTTLE, PLASTIC (51655-477-52) | 30 tablet | 2022-12-02 | No | No | Current |