hydrochlorothiazide
- Product NDC
- 68071-1255
- 11-digit product format
- 680711255
- Labeler code
- 68071
- Product ID
- 68071-1255_4b7dc048-4532-3bd4-e054-00144ff88e88
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- hydrochlorothiazide
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA090510
- Marketing category
- ANDA
- Marketing start
- 2010-03-15
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68071-1255-3 | hydrochlorothiazide | 30 in 1 BOTTLE | CAPSULE | 30 | | 1 |
| 68071-1255-6 | hydrochlorothiazide | 60 in 1 BOTTLE | CAPSULE | 60 | | 1 |
| 68071-1255-9 | hydrochlorothiazide | 90 in 1 BOTTLE | CAPSULE | 90 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68071-1255 | HYDROCHLOROTHIAZIDE CAPSULE [NUCARE PHARMACEUTICALS, INC.] | 1 | Legacy NDC, 3 package rows | 20170324_4b7dbff8-c9ad-1d20-e054-00144ff8d46c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 68071-1255-3 | 68071125503 | 30 in 1 BOTTLE | Historical |
| 68071-1255-6 | 68071125506 | 60 in 1 BOTTLE | Historical |
| 68071-1255-9 | 68071125509 | 90 in 1 BOTTLE | Historical |