Captopril
- Product NDC
- 0781-8052
- 11-digit product format
- 007818052
- Labeler code
- 0781
- Product ID
- 0781-8052_d3b1f9c2-fa3b-4326-8561-507a20256520
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Captopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- SANDOZ INC.
- Application
- ANDA074477
- Marketing category
- ANDA
- Marketing start
- 2016-07-01
- Marketing end
- 0000-00-00
- Substance
- CAPTOPRIL
- Active strength
- 13 mg/1
- Pharmacologic classes
- Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
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 |
|---|
| 0781-8052-01 | 00781805201 | 100 TABLET in 1 BOTTLE (0781-8052-01) | 100 tablet | 2016-07-01 | 0000-00-00 | No | No | Current |
| 0781-8052-10 | 00781805210 | 1000 TABLET in 1 BOTTLE (0781-8052-10) | 1000 tablet | 2016-07-01 | 0000-00-00 | No | No | Current |