Quinapril Hydrochloride and Hydrochlorothiazide
- Product NDC
- 31722-375
- 11-digit product format
- 317220375
- Labeler code
- 31722
- Product ID
- 31722-375_d32a5dbc-7a55-421a-bf8d-68dbb6eb8c3d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Quinapril Hydrochloride and Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Camber Pharmaceuticals
- Application
- ANDA201356
- Marketing category
- ANDA
- Marketing start
- 2011-12-15
- Marketing end
- 0000-00-00
- Substance
- QUINAPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
- Active strength
- 20 mg/1; mg/1
- Pharmacologic classes
- Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],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 |
|---|
| 31722-375-90 | Quinapril Hydrochloride and Hydrochlorothiazide | 90 in 1 BOTTLE | TABLET | 90 | | 8 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 31722-375 | QUINAPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE TABLET [CAMBER PHARMACEUTICALS] | 8 | Legacy NDC, 1 package rows | 20151014_7e97959c-d34d-4a6e-99f0-a821d5ce5089.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 31722-375-90 | 31722037590 | 90 in 1 BOTTLE | Historical |