Metolazone
- Product NDC
- 63629-8722
- 11-digit product format
- 636298722
- Labeler code
- 63629
- Product ID
- 63629-8722_1c9bb8dd-aaa5-401f-bde3-122a543a5fd7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metolazone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA076732
- Marketing category
- ANDA
- Marketing start
- 2003-12-19
- 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 |
|---|
| 63629-8722-1 | 63629872201 | 100 TABLET in 1 BOTTLE (63629-8722-1) | 100 tablet | 2021-08-19 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Metolazone Tablets, USP | Bryant Ranch Prepack | 2023-11-01 | HUMAN PRESCRIPTION DRUG LABEL | 102 |