AMINOCAPROIC ACID
- Product NDC
- 80005-128
- 11-digit product format
- 800050128
- Labeler code
- 80005
- Product ID
- 80005-128_98b3715d-7fcf-4802-8b34-c1296b03b5fb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- AMINOCAPROIC ACID
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Carnegie Pharmaceuticals, LLC
- Application
- ANDA213928
- Marketing category
- ANDA
- Marketing start
- 2021-03-15
- Substance
- AMINOCAPROIC ACID
- Active strength
- 500 mg/1
- 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 | 500 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | U6F3787206 |
| Rxcui | 197351, 476271 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 80005-128-08 | AMINOCAPROIC ACID | 30 in 1 BOTTLE | TABLET | 30 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 80005-128 | AMINOCAPROIC ACID TABLET [CARNEGIE PHARMACEUTICALS, LLC] | 3 | Current NDC, Legacy NDC, 1 package rows | 20230422_871ec401-30f8-4154-a16e-b82dc1e04b49.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 80005-128-08 | 80005012808 | 30 TABLET in 1 BOTTLE (80005-128-08) | 30 tablet | 2021-03-15 | 0000-00-00 | No | No | Current |