hydrochlorothiazide
- Product NDC
- 70518-1676
- 11-digit product format
- 705181676
- Labeler code
- 70518
- Product ID
- 70518-1676_e5cedec4-98fa-7aa2-e053-2995a90a5ae0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- hydrochlorothiazide
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA090510
- Marketing category
- ANDA
- Marketing start
- 2018-11-16
- Marketing end
- 0000-00-00
- Substance
- HYDROCHLOROTHIAZIDE
- Active strength
- 13 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 |
|---|
| 70518-1676-1 | 70518167601 | 60 CAPSULE in 1 BLISTER PACK (70518-1676-1) | 60 capsule | 2022-05-31 | 0000-00-00 | No | No | Current |
| 70518-1676-2 | 70518167602 | 100 POUCH in 1 BOX (70518-1676-2) > 1 CAPSULE in 1 POUCH (70518-1676-3) | 100 pouch | 2022-06-15 | 0000-00-00 | No | No | Current |