Aminocaproic Acid
- Product NDC
- 62559-225
- 11-digit product format
- 625590225
- Labeler code
- 62559
- Product ID
- 62559-225_69d62441-f780-44a9-91aa-43d3285b5b34
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Aminocaproic Acid
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- ANI Pharmaceuticals, Inc.
- Application
- ANDA211629
- Marketing category
- ANDA
- Marketing start
- 2020-12-16
- Marketing end
- 0000-00-00
- Substance
- AMINOCAPROIC ACID
- Active strength
- 500 mg/1
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 62559-225 | AMINOCAPROIC ACID TABLET [ANI PHARMACEUTICALS, INC.] | 3 | Legacy NDC | 20241116_73bbf009-b07d-49df-b548-721a6451d9e3.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 62559-225-30 | 62559022530 | 30 TABLET in 1 BOTTLE (62559-225-30) | 30 tablet | 2020-12-16 | 0000-00-00 | No | No | Current |