Metolazone
- Product NDC
- 43353-999
- 11-digit product format
- 433530999
- Labeler code
- 43353
- Product ID
- 43353-999_484ad518-75e8-4281-a8f2-17d745567d44
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- metolazone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- NDA017386
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 1973-11-27
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 43353-999 | METOLAZONE TABLET [APHENA PHARMA SOLUTIONS - TENNESSEE, LLC] | 1 | Legacy NDC | 20160707_41aa6704-f3c4-4174-b74d-df2223bdf791.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43353-999-09 | 43353099909 | 9000 TABLET in 1 BOTTLE, PLASTIC (43353-999-09) | 9000 tablet | 2015-02-22 | 0000-00-00 | No | No | Current |