Aminocaproic Acid
- Product NDC
- 71872-7359
- 11-digit product format
- 718727359
- Labeler code
- 71872
- Product ID
- 71872-7359_4629d7c3-8a2c-46d6-e063-6294a90a7354
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- AMINOCAPROIC ACID
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Medical Purchasing Solutions, LLC
- Application
- ANDA070010
- Marketing category
- ANDA
- Marketing start
- 2010-05-12
- Substance
- AMINOCAPROIC ACID
- Active strength
- 250 mg/mL
- Pharmacologic classes
- Antifibrinolytic Agent [EPC], Decreased Fibrinolysis [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Aminocaproic Acid
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| AMINOCAPROIC ACID | 250 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | U6F3787206 |
| Rxcui | 1718760 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71872-7359-1 | Aminocaproic Acid | 1 in 1 BAG | INJECTION, SOLUTION | 1 | | 1 |
| 71872-7359-1 | Aminocaproic Acid | 20 mL in 1 VIAL, SINGLE-DOSE | INJECTION, SOLUTION | 20 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 71872-7359-1 | 71872735901 | 1 VIAL, SINGLE-DOSE in 1 BAG (71872-7359-1) / 20 mL in 1 VIAL, SINGLE-DOSE | 2025-09-11 | No | No | Historical |