LOSARTAN POT/HCTZ
- Product NDC
- 61919-873
- 11-digit product format
- 619190873
- Labeler code
- 61919
- Product ID
- 61919-873_8f28d40c-450f-5eeb-e053-2a95a90a932f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LOSARTAN POT/HCTZ
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA091629
- Marketing category
- ANDA
- Marketing start
- 2019-06-05
- Marketing end
- 0000-00-00
- Substance
- LOSARTAN POTASSIUM; HYDROCHLOROTHIAZIDE
- Active strength
- 100 mg/1; mg/1
- Pharmacologic classes
- Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 61919-873-90 | LOSARTAN POT/HCTZ | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61919-873 | LOSARTAN POT/HCTZ TABLET, FILM COATED [DIRECT_RX] | 2 | Legacy NDC, 1 package rows | 20190803_8a99337b-ac1f-27c2-e053-2a95a90a4bd6.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 61919-873-90 | 61919087390 | 90 TABLET, FILM COATED in 1 BOTTLE (61919-873-90) | 2019-06-05 | 0000-00-00 | No | No | Current |