Metolazone
- Product NDC
- 68151-2939
- 11-digit product format
- 681512939
- Labeler code
- 68151
- Product ID
- 68151-2939_8f14f89c-25a2-406e-8b85-72dfd0763dfa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- metolazone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Carilion Materials Management
- Application
- ANDA076698
- Marketing category
- ANDA
- Marketing start
- 2004-10-19
- Marketing end
- 0000-00-00
- Substance
- METOLAZONE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Increased Diuresis [PE],Thiazide-like Diuretic [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68151-2939-0 | Metolazone | 1 in 1 PACKAGE | TABLET | 1 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68151-2939 | METOLAZONE TABLET [CARILION MATERIALS MANAGEMENT] | 5 | Legacy NDC, 1 package rows | 20171229_e535c22d-ffe7-4adc-b188-9efe4cb580a9.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 68151-2939-0 | 68151293900 | 1 in 1 PACKAGE | Historical |