hydrochlorothiazide
- Product NDC
- 70518-0335
- 11-digit product format
- 705180335
- Labeler code
- 70518
- Product ID
- 70518-0335_ea3a4f49-8ba9-37c6-e053-2995a90af96b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- hydrochlorothiazide
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA090510
- Marketing category
- ANDA
- Marketing start
- 2017-03-17
- 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 |
|---|
| 70518-0335-0 | 70518033500 | 30 CAPSULE in 1 BLISTER PACK (70518-0335-0) | 30 capsule | 2017-03-17 | 0000-00-00 | No | No | Current |
| 70518-0335-1 | 70518033501 | 90 CAPSULE in 1 BOTTLE, PLASTIC (70518-0335-1) | 90 capsule | 2017-05-24 | 0000-00-00 | No | No | Current |
| 70518-0335-2 | 70518033502 | 60 CAPSULE in 1 BLISTER PACK (70518-0335-2) | 60 capsule | 2019-04-02 | 0000-00-00 | No | No | Current |