METOLAZONE
- Product NDC
- 50090-6972
- 11-digit product format
- 500906972
- Labeler code
- 50090
- Product ID
- 50090-6972_08a08e21-404b-4d25-8672-c4a6ae59b662
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- METOLAZONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA215184
- Marketing category
- ANDA
- Marketing start
- 2021-08-20
- 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 |
|---|
| 50090-6972-0 | 50090697200 | 30 TABLET in 1 BOTTLE (50090-6972-0) | 30 tablet | 2023-12-21 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Metolazone Tablets, USP | A-S Medication Solutions | 2023-12-27 | HUMAN PRESCRIPTION DRUG LABEL | 1 |