Hydrochlorothiazide
- Product NDC
- 42291-315
- 11-digit product format
- 422910315
- Labeler code
- 42291
- Product ID
- 42291-315_d57aad30-732c-2203-e053-2a95a90aeb0c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- CAPSULE, GELATIN COATED
- Route
- ORAL
- Labeler
- AvKARE
- Application
- ANDA078391
- Marketing category
- ANDA
- Marketing start
- 2016-09-12
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 42291-315-10 | 42291031510 | 1000 CAPSULE, GELATIN COATED in 1 BOTTLE (42291-315-10) | 2016-09-12 | 0000-00-00 | No | No | Current |
| 42291-315-90 | 42291031590 | 90 CAPSULE, GELATIN COATED in 1 BOTTLE (42291-315-90) | 2016-09-12 | 0000-00-00 | No | No | Current |