QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE
- Product NDC
- 65862-161
- 11-digit product format
- 658620161
- Labeler code
- 65862
- Product ID
- 65862-161_5842ecc2-874a-481b-8997-afa9d862dc5d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Aurobindo Pharma Limited
- Application
- ANDA078450
- Marketing category
- ANDA
- Marketing start
- 2007-08-24
- Substance
- HYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDE
- Active strength
- 12.5; 10 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
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| QUINAPRIL HYDROCHLORIDE | 12.5 mg/1 |
| HYDROCHLOROTHIAZIDE | 10 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 33067B3N2M, 0J48LPH2TH |
| Rxcui | 310796, 310797, 310809 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 65862-161-90 | QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | | 24 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| HYDROCHLOROTHIAZIDE | ACTIVE INGREDIENT | 0J48LPH2TH | QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE TABLET, FILM COATED [AUROBINDO PHARMA LIMITED] | 13 | |
| QUINAPRIL HYDROCHLORIDE | ACTIVE INGREDIENT | 33067B3N2M | QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE TABLET, FILM COATED [AUROBINDO PHARMA LIMITED] | 13 | |
| HYDROCHLOROTHIAZIDE | ACTIVE MOIETY | 0J48LPH2TH | QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE TABLET, FILM COATED [AUROBINDO PHARMA LIMITED] | 13 | |
| QUINAPRILAT | ACTIVE MOIETY | 34SSX5LDE5 | QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE TABLET, FILM COATED [AUROBINDO PHARMA LIMITED] | 13 | |
| CROSPOVIDONE | INACTIVE INGREDIENT | 68401960MK | QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE TABLET, FILM COATED [AUROBINDO PHARMA LIMITED] | 13 | |
| FERRIC OXIDE RED | INACTIVE INGREDIENT | 1K09F3G675 | QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE TABLET, FILM COATED [AUROBINDO PHARMA LIMITED] | 13 | |
| FERRIC OXIDE YELLOW | INACTIVE INGREDIENT | EX438O2MRT | QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE TABLET, FILM COATED [AUROBINDO PHARMA LIMITED] | 13 | |
| HYDROXYPROPYL CELLULOSE (TYPE H) | INACTIVE INGREDIENT | RFW2ET671P | QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE TABLET, FILM COATED [AUROBINDO PHARMA LIMITED] | 13 | |
| HYPROMELLOSE 2910 (3 MPA.S) | INACTIVE INGREDIENT | 0VUT3PMY82 | QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE TABLET, FILM COATED [AUROBINDO PHARMA LIMITED] | 13 | |
| HYPROMELLOSE 2910 (50 MPA.S) | INACTIVE INGREDIENT | 1IVH67816N | QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE TABLET, FILM COATED [AUROBINDO PHARMA LIMITED] | 13 | |
| LACTOSE MONOHYDRATE | INACTIVE INGREDIENT | EWQ57Q8I5X | QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE TABLET, FILM COATED [AUROBINDO PHARMA LIMITED] | 13 | |
| MAGNESIUM CARBONATE | INACTIVE INGREDIENT | 0E53J927NA | QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE TABLET, FILM COATED [AUROBINDO PHARMA LIMITED] | 13 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE TABLET, FILM COATED [AUROBINDO PHARMA LIMITED] | 13 | |
| POLYETHYLENE GLYCOL 400 | INACTIVE INGREDIENT | B697894SGQ | QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE TABLET, FILM COATED [AUROBINDO PHARMA LIMITED] | 13 | |
| POVIDONE K30 | INACTIVE INGREDIENT | U725QWY32X | QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE TABLET, FILM COATED [AUROBINDO PHARMA LIMITED] | 13 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE TABLET, FILM COATED [AUROBINDO PHARMA LIMITED] | 13 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 65862-161 | QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE TABLET, FILM COATED [AUROBINDO PHARMA LIMITED] | 24 | Current NDC, Legacy NDC, 1 package rows | 20240430_50a58159-9572-4445-9859-b392632597da.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 65862-161-90 | 65862016190 | 90 TABLET, FILM COATED in 1 BOTTLE (65862-161-90) | 2007-08-24 | 0000-00-00 | No | No | Current |