Chlorthalidone
- Product NDC
- 63629-8761
- 11-digit product format
- 636298761
- Labeler code
- 63629
- Product ID
- 63629-8761_a7f7f7d2-4915-4a44-9033-c9b2ce9f22b6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlorthalidone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA213412
- Marketing category
- ANDA
- Marketing start
- 2020-02-13
- Substance
- CHLORTHALIDONE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Increased Diuresis [PE], Thiazide-like Diuretic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
openFDA Listing Details
- Product ID
- 63629-8761_a7f7f7d2-4915-4a44-9033-c9b2ce9f22b6
- Product type
- HUMAN PRESCRIPTION DRUG
- Finished product
- Yes
- Brand name base
- Chlorthalidone
- Generic name
- Chlorthalidone
- Dosage form
- TABLET
- Route
- ORAL
- Marketing start
- 2020-02-13
- Marketing category
- ANDA
- Application number
- ANDA213412
- Pharmacologic classes
- Increased Diuresis [PE]; Thiazide-like Diuretic [EPC]
- Listing expiration
- 2026-12-31
openFDA Active Ingredients
| Ingredient | Strength |
|---|
| CHLORTHALIDONE | 25 mg/1 |
openFDA Harmonized Identifiers
| Field | Values |
|---|
| Unii | Q0MQD1073Q |
| Rxcui | 197499 |
| Spl Set Id | a1ab541b-7515-4888-b3e0-aca52875562d |
| Manufacturer Name | Bryant Ranch Prepack |
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| Q0MQD1073Q | CHLORTHALIDONE | 77-36-1 | CHLORTHALIDONE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-8761-1 | 63629876101 | 100 TABLET in 1 BOTTLE (63629-8761-1) | 100 tablet | 2020-02-13 | 0000-00-00 | No | No | Current |