Quinapril
- Product NDC
- 65862-618
- 11-digit product format
- 658620618
- Labeler code
- 65862
- Product ID
- 65862-618_5263abd5-ce46-4918-9bb0-9632861bcbc9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Quinapril Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Aurobindo Pharma Limited
- Application
- ANDA202725
- Marketing category
- ANDA
- Marketing start
- 2013-04-29
- Substance
- QUINAPRIL HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Quinapril
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| QUINAPRIL HYDROCHLORIDE | 10 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 33067B3N2M |
| Rxcui | 312748, 312749, 312750, 314203 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 65862-618-10 | Quinapril | 10 in 1 BLISTER PACK | TABLET, FILM COATED | 10 | | 14 |
| 65862-618-30 | Quinapril | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 14 |
| 65862-618-55 | Quinapril | 15000 in 1 BOTTLE | TABLET, FILM COATED | 15000 | | 14 |
| 65862-618-78 | Quinapril | 10 in 1 CARTON | TABLET, FILM COATED | 10 | | 14 |
| 65862-618-90 | Quinapril | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | | 14 |
| 65862-618-99 | Quinapril | 1000 in 1 BOTTLE | TABLET, FILM COATED | 1000 | | 14 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| QUINAPRIL HYDROCHLORIDE | ACTIVE INGREDIENT | 33067B3N2M | QUINAPRIL (QUINAPRIL HYDROCHLORIDE) TABLET, FILM COATED [AUROBINDO PHARMA LIMITED] | 6 | |
| QUINAPRILAT | ACTIVE MOIETY | 34SSX5LDE5 | QUINAPRIL (QUINAPRIL HYDROCHLORIDE) TABLET, FILM COATED [AUROBINDO PHARMA LIMITED] | 6 | |
| CROSPOVIDONE | INACTIVE INGREDIENT | 68401960MK | QUINAPRIL (QUINAPRIL HYDROCHLORIDE) TABLET, FILM COATED [AUROBINDO PHARMA LIMITED] | 6 | |
| FERRIC OXIDE RED | INACTIVE INGREDIENT | 1K09F3G675 | QUINAPRIL (QUINAPRIL HYDROCHLORIDE) TABLET, FILM COATED [AUROBINDO PHARMA LIMITED] | 6 | |
| HYDROXYPROPYL CELLULOSE (TYPE H) | INACTIVE INGREDIENT | RFW2ET671P | QUINAPRIL (QUINAPRIL HYDROCHLORIDE) TABLET, FILM COATED [AUROBINDO PHARMA LIMITED] | 6 | |
| HYPROMELLOSE 2910 (3 MPA.S) | INACTIVE INGREDIENT | 0VUT3PMY82 | QUINAPRIL (QUINAPRIL HYDROCHLORIDE) TABLET, FILM COATED [AUROBINDO PHARMA LIMITED] | 6 | |
| HYPROMELLOSE 2910 (50 MPA.S) | INACTIVE INGREDIENT | 1IVH67816N | QUINAPRIL (QUINAPRIL HYDROCHLORIDE) TABLET, FILM COATED [AUROBINDO PHARMA LIMITED] | 6 | |
| LACTOSE MONOHYDRATE | INACTIVE INGREDIENT | EWQ57Q8I5X | QUINAPRIL (QUINAPRIL HYDROCHLORIDE) TABLET, FILM COATED [AUROBINDO PHARMA LIMITED] | 6 | |
| MAGNESIUM CARBONATE | INACTIVE INGREDIENT | 0E53J927NA | QUINAPRIL (QUINAPRIL HYDROCHLORIDE) TABLET, FILM COATED [AUROBINDO PHARMA LIMITED] | 6 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | QUINAPRIL (QUINAPRIL HYDROCHLORIDE) TABLET, FILM COATED [AUROBINDO PHARMA LIMITED] | 6 | |
| POLYETHYLENE GLYCOL 400 | INACTIVE INGREDIENT | B697894SGQ | QUINAPRIL (QUINAPRIL HYDROCHLORIDE) TABLET, FILM COATED [AUROBINDO PHARMA LIMITED] | 6 | |
| POVIDONE K30 | INACTIVE INGREDIENT | U725QWY32X | QUINAPRIL (QUINAPRIL HYDROCHLORIDE) TABLET, FILM COATED [AUROBINDO PHARMA LIMITED] | 6 | |
| SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | QUINAPRIL (QUINAPRIL HYDROCHLORIDE) TABLET, FILM COATED [AUROBINDO PHARMA LIMITED] | 6 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | QUINAPRIL (QUINAPRIL HYDROCHLORIDE) TABLET, FILM COATED [AUROBINDO PHARMA LIMITED] | 6 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 65862-618 | QUINAPRIL (QUINAPRIL HYDROCHLORIDE) TABLET, FILM COATED [AUROBINDO PHARMA LIMITED] | 14 | Current NDC, Legacy NDC, 6 package rows | 20240517_93e6e668-5306-4f26-81d8-cbc3a7a5e787.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 65862-618-10 | 65862061810 | 10 in 1 BLISTER PACK | | | | | | Historical |
| 65862-618-30 | 65862061830 | 30 TABLET, FILM COATED in 1 BOTTLE (65862-618-30) | | 2013-04-29 | 0000-00-00 | No | No | Current |
| 65862-618-55 | 65862061855 | 15000 TABLET, FILM COATED in 1 BOTTLE (65862-618-55) | | 2013-04-29 | 0000-00-00 | No | No | Current |
| 65862-618-78 | 65862061878 | 10 BLISTER PACK in 1 CARTON (65862-618-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-618-10) | 10 blister pack | 2013-04-29 | 0000-00-00 | No | No | Current |
| 65862-618-90 | 65862061890 | 90 TABLET, FILM COATED in 1 BOTTLE (65862-618-90) | | 2013-04-29 | 0000-00-00 | No | No | Current |
| 65862-618-99 | 65862061899 | 1000 TABLET, FILM COATED in 1 BOTTLE (65862-618-99) | | 2013-04-29 | 0000-00-00 | No | No | Current |