Hydrochlorothiazide
- Product NDC
- 10544-544
- 11-digit product format
- 105440544
- Labeler code
- 10544
- Product ID
- 10544-544_d19b12e4-5227-4b67-99a7-2a255d0fdf53
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Blenheim Pharmacal, Inc.
- Application
- ANDA079237
- Marketing category
- ANDA
- Marketing start
- 2013-10-07
- 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
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 10544-544-90 | 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 |
|---|
| 10544-544 | HYDROCHLOROTHIAZIDE CAPSULE [BLENHEIM PHARMACAL, INC.] | 1 | Legacy NDC, 1 package rows | 20160113_209b1202-c3a8-4f2b-93c6-60fe37a2011f.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 10544-544-90 | 10544054490 | 90 in 1 BOTTLE | Historical |