Aminocaproic acid
- Product NDC
- 60687-529
- 11-digit product format
- 606870529
- Labeler code
- 60687
- Product ID
- 60687-529_e87dbc31-1aa9-6897-e053-2995a90a9ff1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Aminocaproic acid
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA212780
- Marketing category
- ANDA
- Marketing start
- 2022-10-20
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60687-529-36 | 60687052936 | 2 TRAY in 1 CASE (60687-529-36) > 10 CUP, UNIT-DOSE in 1 TRAY (60687-529-46) > 5 mL in 1 CUP, UNIT-DOSE (60687-529-40) | 2 tray | 2022-10-20 | 0000-00-00 | No | No | Current |