Hydrochlorothiazide
- Product NDC
- 70518-0597
- 11-digit product format
- 705180597
- Labeler code
- 70518
- Product ID
- 70518-0597_e9595624-35a7-373e-e053-2995a90a16a4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA083177
- Marketing category
- ANDA
- Marketing start
- 2017-06-28
- Marketing end
- 0000-00-00
- Substance
- HYDROCHLOROTHIAZIDE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-0597-1 | 70518059701 | 100 POUCH in 1 BOX (70518-0597-1) > 1 TABLET in 1 POUCH (70518-0597-2) | 100 pouch | 2022-06-15 | 0000-00-00 | No | No | Current |