Quinapril
- Product NDC
- 63629-1241
- 11-digit product format
- 636291241
- Labeler code
- 63629
- Product ID
- 63629-1241_1d295d65-ebf9-440e-aa59-747418d09ce0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Quinapril
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA075504
- Marketing category
- ANDA
- Marketing start
- 2010-02-25
- 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
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 63629-1241-1 | 2021-07-01 | C162847 | 48780-1 | 9855d018-e270-cd31-e053-dbdaa90ab51a | 7d1baabb-27c8-49b7-9a03-0891114ba111 |
| 63629-1241-2 | 2021-07-01 | C162847 | 48780-1 | 9855d018-e270-cd31-e053-dbdaa90ab51a | 7d1baabb-27c8-49b7-9a03-0891114ba111 |
| 63629-1241-1 | 2019-11-27 | C162847 | 48780-1 | 9855d018-e270-cd31-e053-dbdaa90ab51a | 7d1baabb-27c8-49b7-9a03-0891114ba111 |
| 63629-1241-2 | 2019-11-27 | C162847 | 48780-1 | 9855d018-e270-cd31-e053-dbdaa90ab51a | 7d1baabb-27c8-49b7-9a03-0891114ba111 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 63629-1241-1 | EA - Each | 63629-1241 | e8d9d09b-6c5a-471a-9455-47cac16dd4ce | 1 | 2012-07-24 |