Metolazone
- Product NDC
- 60687-547
- 11-digit product format
- 606870547
- Labeler code
- 60687
- Product ID
- 60687-547_e28395b4-4448-47cc-e053-2995a90a9edd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metolazone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- NDA017386
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2020-05-01
- Marketing end
- 2023-06-30
- Substance
- METOLAZONE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Increased Diuresis [PE], Thiazide-like Diuretic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60687-547-01 | 60687054701 | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-547-01) > 1 TABLET in 1 BLISTER PACK (60687-547-11) | 100 blister pack | 2020-05-01 | 0000-00-00 | No | No | Current |