AMINOCAPROIC ACID
- Product NDC
- 24658-798
- 11-digit product format
- 246580798
- Labeler code
- 24658
- Product ID
- 24658-798_2b368d9c-2024-fecb-e063-6294a90aa87b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- AMINOCAPROIC ACID
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PURACAP LABORATORIES LLC DBA BLU PHARMACEUTICALS
- Application
- ANDA213928
- Marketing category
- ANDA
- Marketing start
- 2023-01-24
- 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 |
|---|
| 24658-798-30 | AMINOCAPROIC ACID | 30 in 1 BOTTLE | TABLET | 30 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 24658-798 | AMINOCAPROIC ACID TABLET [PURACAP LABORATORIES LLC DBA BLU PHARMACEUTICALS] | 2 | Current NDC, 1 package rows | 20250110_7d08ad63-71f5-4286-9622-84295668a293.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 24658-798-30 | 24658079830 | 30 TABLET in 1 BOTTLE (24658-798-30) | 30 tablet | 2023-01-24 | No | No | Current |