Captopril
- Product NDC
- 63629-8730
- 11-digit product format
- 636298730
- Labeler code
- 63629
- Product ID
- 63629-8730_3b69b42f-96f1-4f3d-ade7-6eeb47c87f6d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Captopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA074477
- Marketing category
- ANDA
- Marketing start
- 2016-07-01
- Marketing end
- 0000-00-00
- Substance
- CAPTOPRIL
- Active strength
- 100 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 Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63629-8730 | CAPTOPRIL TABLET [BRYANT RANCH PREPACK] | 102 | Legacy NDC | 20240112_23b1f2f5-2d84-4a1e-997f-6489204878b2.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-8730-1 | 63629873001 | 100 TABLET in 1 BOTTLE (63629-8730-1) | 100 tablet | 2021-08-19 | 0000-00-00 | No | No | Current |