Quinapril
- Product NDC
- 68180-558
- 11-digit product format
- 681800558
- Labeler code
- 68180
- Product ID
- 68180-558_a9598a21-6f99-4c86-ace6-b5638da2bec8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Quinapril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lupin Pharmaceuticals, Inc.
- Application
- ANDA077690
- Marketing category
- ANDA
- Marketing start
- 2007-02-26
- Substance
- QUINAPRIL HYDROCHLORIDE
- Active strength
- 20 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 | 20 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 |
|---|
| 68180-558-03 | Quinapril | 1000 in 1 BOTTLE | TABLET | 1000 | | 17 |
| 68180-558-09 | Quinapril | 90 in 1 BOTTLE | TABLET | 90 | | 17 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| QUINAPRIL HYDROCHLORIDE | ACTIVE INGREDIENT | 33067B3N2M | QUINAPRIL TABLET [LUPIN PHARMACEUTICALS, INC.] | 7 | |
| QUINAPRILAT | ACTIVE MOIETY | 34SSX5LDE5 | QUINAPRIL TABLET [LUPIN PHARMACEUTICALS, INC.] | 7 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | QUINAPRIL TABLET [LUPIN PHARMACEUTICALS, INC.] | 7 | |
| CROSPOVIDONE | INACTIVE INGREDIENT | 68401960MK | QUINAPRIL TABLET [LUPIN PHARMACEUTICALS, INC.] | 7 | |
| FERRIC OXIDE YELLOW | INACTIVE INGREDIENT | EX438O2MRT | QUINAPRIL TABLET [LUPIN PHARMACEUTICALS, INC.] | 7 | |
| LECITHIN, SOYBEAN | INACTIVE INGREDIENT | 1DI56QDM62 | QUINAPRIL TABLET [LUPIN PHARMACEUTICALS, INC.] | 7 | |
| MAGNESIUM CARBONATE | INACTIVE INGREDIENT | 0E53J927NA | QUINAPRIL TABLET [LUPIN PHARMACEUTICALS, INC.] | 7 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | QUINAPRIL TABLET [LUPIN PHARMACEUTICALS, INC.] | 7 | |
| POLYVINYL ALCOHOL | INACTIVE INGREDIENT | 532B59J990 | QUINAPRIL TABLET [LUPIN PHARMACEUTICALS, INC.] | 7 | |
| POVIDONE | INACTIVE INGREDIENT | FZ989GH94E | QUINAPRIL TABLET [LUPIN PHARMACEUTICALS, INC.] | 7 | |
| TALC | INACTIVE INGREDIENT | 7SEV7J4R1U | QUINAPRIL TABLET [LUPIN PHARMACEUTICALS, INC.] | 7 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | QUINAPRIL TABLET [LUPIN PHARMACEUTICALS, INC.] | 7 | |
| XANTHAN GUM | INACTIVE INGREDIENT | TTV12P4NEE | QUINAPRIL TABLET [LUPIN PHARMACEUTICALS, INC.] | 7 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68180-558 | QUINAPRIL TABLET [LUPIN PHARMACEUTICALS, INC.] | 17 | Current NDC, Legacy NDC, 2 package rows | 20231215_8ded0773-3aec-4e89-9836-d22a5a84abf0.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 |
|---|
| 68180-558-03 | 68180055803 | 1000 TABLET in 1 BOTTLE (68180-558-03) | 1000 tablet | 2007-02-26 | 0000-00-00 | No | No | Current |
| 68180-558-09 | 68180055809 | 90 TABLET in 1 BOTTLE (68180-558-09) | 90 tablet | 2007-02-26 | 0000-00-00 | No | No | Current |