AMINOCAPROIC ACID
- Product NDC
- 69315-503
- 11-digit product format
- 693150503
- Labeler code
- 69315
- Product ID
- 69315-503_7c66aebb-36c0-412d-b587-5c7580a5feca
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- AMINOCAPROIC ACID
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Leading Pharma, LLC
- Application
- ANDA214140
- Marketing category
- ANDA
- Marketing start
- 2021-03-18
- Marketing end
- 0000-00-00
- Substance
- AMINOCAPROIC ACID
- Active strength
- 0 g/mL
- Pharmacologic classes
- Antifibrinolytic Agent [EPC],Decreased Fibrinolysis [PE]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69315-503-24 | 69315050324 | 236.5 mL in 1 BOTTLE (69315-503-24) | 236.5 ml | 2021-03-18 | 0000-00-00 | No | No | Current |