Lisinopril and hydrochlorothiazide
- Product NDC
- 21695-733
- 11-digit product format
- 216950733
- Labeler code
- 21695
- Product ID
- 21695-733_63fa5147-fb3e-47ec-bea1-a80e1f551866
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lisinopril and hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Rebel Distributors Corp
- Application
- ANDA076194
- Marketing category
- ANDA
- Marketing start
- 2003-03-01
- Marketing end
- 0000-00-00
- Substance
- LISINOPRIL; HYDROCHLOROTHIAZIDE
- Active strength
- 10 mg/1; 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 |
|---|
| 21695-733-30 | Lisinopril and hydrochlorothiazide | 30 in 1 BOTTLE, PLASTIC | TABLET | 30 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 21695-733 | LISINOPRIL AND HYDROCHLOROTHIAZIDE TABLET [REBEL DISTRIBUTORS CORP] | 1 | Legacy NDC, 1 package rows | 20101119_63fa5147-fb3e-47ec-bea1-a80e1f551866.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 21695-733-30 | 21695073330 | 30 in 1 BOTTLE, PLASTIC | Historical |