Metolazone
- Product NDC
- 50090-6802
- 11-digit product format
- 500906802
- Labeler code
- 50090
- Product ID
- 50090-6802_bef7bd92-1e16-40d7-8158-1ef956cd843f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metolazone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA213827
- Marketing category
- ANDA
- Marketing start
- 2021-05-15
- Substance
- METOLAZONE
- Active strength
- 2.5 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 |
|---|
| 50090-6802-0 | 50090680200 | 30 TABLET in 1 BOTTLE (50090-6802-0) | 30 tablet | 2023-11-06 | No | No | Historical |