Accupril
- Product NDC
- 0071-0532
- 11-digit product format
- 000710532
- Labeler code
- 0071
- Product ID
- 0071-0532_140c689b-e8c8-4db9-9bcf-c68869e0d762
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- quinapril hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Parke-Davis Div of Pfizer Inc
- Application
- NDA019885
- Marketing category
- NDA
- Marketing start
- 1991-11-19
- Marketing end
- 0000-00-00
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| QUINAPRIL HYDROCHLORIDE | ACTIVE INGREDIENT | 33067B3N2M | ACCUPRIL (QUINAPRIL HYDROCHLORIDE) TABLET, FILM COATED [PARKE-DAVIS DIV OF PFIZER INC] | 13 | |
| QUINAPRILAT | ACTIVE MOIETY | 34SSX5LDE5 | ACCUPRIL (QUINAPRIL HYDROCHLORIDE) TABLET, FILM COATED [PARKE-DAVIS DIV OF PFIZER INC] | 13 | |
| CANDELILLA WAX | INACTIVE INGREDIENT | WL0328HX19 | ACCUPRIL (QUINAPRIL HYDROCHLORIDE) TABLET, FILM COATED [PARKE-DAVIS DIV OF PFIZER INC] | 13 | |
| CROSPOVIDONE | INACTIVE INGREDIENT | 68401960MK | ACCUPRIL (QUINAPRIL HYDROCHLORIDE) TABLET, FILM COATED [PARKE-DAVIS DIV OF PFIZER INC] | 13 | |
| FERRIC OXIDE RED | INACTIVE INGREDIENT | 1K09F3G675 | ACCUPRIL (QUINAPRIL HYDROCHLORIDE) TABLET, FILM COATED [PARKE-DAVIS DIV OF PFIZER INC] | 13 | |
| GELATIN | INACTIVE INGREDIENT | 2G86QN327L | ACCUPRIL (QUINAPRIL HYDROCHLORIDE) TABLET, FILM COATED [PARKE-DAVIS DIV OF PFIZER INC] | 13 | |
| LACTOSE | INACTIVE INGREDIENT | J2B2A4N98G | ACCUPRIL (QUINAPRIL HYDROCHLORIDE) TABLET, FILM COATED [PARKE-DAVIS DIV OF PFIZER INC] | 13 | |
| MAGNESIUM CARBONATE | INACTIVE INGREDIENT | 0E53J927NA | ACCUPRIL (QUINAPRIL HYDROCHLORIDE) TABLET, FILM COATED [PARKE-DAVIS DIV OF PFIZER INC] | 13 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | ACCUPRIL (QUINAPRIL HYDROCHLORIDE) TABLET, FILM COATED [PARKE-DAVIS DIV OF PFIZER INC] | 13 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | ACCUPRIL (QUINAPRIL HYDROCHLORIDE) TABLET, FILM COATED [PARKE-DAVIS DIV OF PFIZER INC] | 13 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0071-0532 | ACCUPRIL (QUINAPRIL HYDROCHLORIDE) TABLET, FILM COATED ACCUPRIL (QUINAPRIL) TABLET, FILM COATED [PARKE-DAVIS DIV OF PFIZER INC] | 26 | Legacy NDC | 20250119_63cf5651-d52c-4d27-9fd4-ed9cd9724dff.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0071-0532-23 | 00071053223 | 90 TABLET, FILM COATED in 1 BOTTLE (0071-0532-23) | | 1991-11-19 | 0000-00-00 | No | No | Current |
| 0071-0532-40 | 00071053240 | 100 BLISTER PACK in 1 CARTON (0071-0532-40) > 1 TABLET, FILM COATED in 1 BLISTER PACK | 100 blister pack | 1991-11-19 | 2022-01-31 | No | No | Current |