metolazone
- Product NDC
- 71610-142
- 11-digit product format
- 716100142
- Labeler code
- 71610
- Product ID
- 71610-142_75f1aa5c-c27e-414b-8c23-32122b472bdd
- 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 |
|---|
| 71610-142 | METOLAZONE TABLET [APHENA PHARMA SOLUTIONS - TENNESSEE, LLC] | 1 | Legacy NDC | 20180925_fae89daa-9103-45d8-9966-cd998f258625.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71610-142-09 | 71610014209 | 9000 TABLET in 1 BOTTLE, PLASTIC (71610-142-09) | 9000 tablet | 2018-09-04 | 0000-00-00 | No | No | Current |