Metolazone
- Product NDC
- 72162-1050
- 11-digit product format
- 721621050
- Labeler code
- 72162
- Product ID
- 72162-1050_194df449-f51d-462b-a916-d892e1cf1217
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metolazone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA076466
- Marketing category
- ANDA
- Marketing start
- 2003-12-19
- Substance
- METOLAZONE
- Active strength
- 5 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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| TZ7V40X7VX | METOLAZONE | 17560-51-9 | METOLAZONE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-1050-1 | 72162105001 | 100 TABLET in 1 BOTTLE (72162-1050-1) | 100 tablet | 2024-08-01 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| METOLAZONE TABLETS, USP | Bryant Ranch Prepack | 2024-12-24 | HUMAN PRESCRIPTION DRUG LABEL | 101 |