Aminocaproic Acid
- Product NDC
- 60687-505
- 11-digit product format
- 606870505
- Labeler code
- 60687
- Product ID
- 60687-505_de59572c-b644-a231-e053-2995a90a6b14
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Aminocaproic Acid
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA209060
- Marketing category
- ANDA
- Marketing start
- 2020-05-18
- Marketing end
- 2022-12-31
- Substance
- AMINOCAPROIC ACID
- Active strength
- 500 mg/1
- Pharmacologic classes
- Antifibrinolytic Agent [EPC], Decreased Fibrinolysis [PE]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 60687-505-25 | 60687050525 | 30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-505-25) > 1 TABLET in 1 BLISTER PACK (60687-505-95) | 30 blister pack | 2020-04-15 | 0000-00-00 | No | No | Current |