Losartan potassium and Hydrochlorothiazide
- Product NDC
- 70518-3231
- 11-digit product format
- 705183231
- Labeler code
- 70518
- Product ID
- 70518-3231_cdb1b223-46a4-2686-e053-2a95a90a381f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan potassium and Hydrochlorothiazide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA202289
- Marketing category
- ANDA
- Marketing start
- 2021-10-05
- Marketing end
- 0000-00-00
- Substance
- LOSARTAN POTASSIUM; HYDROCHLOROTHIAZIDE
- Active strength
- 50 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-3231-0 | 70518323100 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3231-0) | 2021-10-05 | 0000-00-00 | No | No | Current |