METOLAZONE
- Product NDC
- 0904-7138
- 11-digit product format
- 009047138
- Labeler code
- 0904
- Product ID
- 0904-7138_822bb0ac-1b6c-4132-afca-d0d0633d1843
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- METOLAZONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA213251
- Marketing category
- ANDA
- Marketing start
- 2020-12-02
- Marketing end
- 0000-00-00
- Substance
- METOLAZONE
- Active strength
- 3 mg/1
- Pharmacologic classes
- Increased Diuresis [PE],Thiazide-like Diuretic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 0904-7138-61 | 00904713861 | 100 BLISTER PACK in 1 CARTON (0904-7138-61) > 1 TABLET in 1 BLISTER PACK | 100 blister pack | 2020-12-02 | 0000-00-00 | No | No | Current |