metolazone
- Product NDC
- 0527-2217
- 11-digit product format
- 005272217
- Labeler code
- 0527
- Product ID
- 0527-2217_fa932ec2-1e68-4e48-a492-ddf5bda15eb2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- metolazone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lannett Company, Inc.
- Application
- NDA017386
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 1973-11-27
- Marketing end
- 2024-01-31
- Substance
- METOLAZONE
- Active strength
- 10 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 |
|---|
| 0527-2217-37 | 00527221737 | 100 TABLET in 1 BOTTLE, PLASTIC (0527-2217-37) | 100 tablet | 1973-11-27 | 0000-00-00 | No | No | Current |