Metolazone
- Product NDC
- 71335-1944
- 11-digit product format
- 713351944
- Labeler code
- 71335
- Product ID
- 71335-1944_34f6150d-961a-94a5-e063-6394a90ad448
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metolazone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA213827
- Marketing category
- ANDA
- Marketing start
- 2021-05-15
- 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 |
|---|
| 71335-1944-1 | 71335194401 | 30 TABLET in 1 BOTTLE (71335-1944-1) | 30 tablet | 2021-09-21 | No | No | Historical |
| 71335-1944-2 | 71335194402 | 90 TABLET in 1 BOTTLE (71335-1944-2) | 90 tablet | 2021-09-21 | No | No | Historical |