QUINAPRIL
- Product NDC
- 71335-1262
- 11-digit product format
- 713351262
- Labeler code
- 71335
- Product ID
- 71335-1262_9fd0b93b-22c0-4813-b02a-41e1235d41cc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- quinapril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA205823
- Marketing category
- ANDA
- Marketing start
- 2016-03-16
- Marketing end
- 0000-00-00
- Substance
- QUINAPRIL HYDROCHLORIDE
- Active strength
- 40 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 Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71335-1262 | QUINAPRIL TABLET [BRYANT RANCH PREPACK] | 100 | Legacy NDC, 4 package rows | 20220225_574cc7ec-537d-42db-8af8-432e6d842aea.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 |
|---|
| 71335-1262-1 | 71335126201 | 30 TABLET in 1 BOTTLE (71335-1262-1) | 30 tablet | 2019-07-05 | 0000-00-00 | No | No | Current |
| 71335-1262-2 | 71335126202 | 60 TABLET in 1 BOTTLE (71335-1262-2) | 60 tablet | 2019-07-05 | 0000-00-00 | No | No | Current |
| 71335-1262-3 | 71335126203 | 90 TABLET in 1 BOTTLE (71335-1262-3) | 90 tablet | 2019-07-05 | 0000-00-00 | No | No | Current |
| 71335-1262-4 | 71335126204 | 180 TABLET in 1 BOTTLE (71335-1262-4) | 180 tablet | 2019-07-05 | 0000-00-00 | No | No | Current |