AMINOCAPROIC ACID
- Product NDC
- 70377-102
- 11-digit product format
- 703770102
- Labeler code
- 70377
- Product ID
- 70377-102_2681dc2f-b544-e29d-90af-ce64675fdd8b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- AMINOCAPROIC ACID
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Biocon Pharma Inc.
- 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 |
|---|
| 70377-102-11 | AMINOCAPROIC ACID | 30 in 1 BOTTLE | TABLET | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70377-102 | AMINOCAPROIC ACID TABLET [BIOCON PHARMA INC.] | 1 | Current NDC, Legacy NDC, 1 package rows | 20220831_9205fb6b-24a0-1138-fd7b-cc33d0df5d6f.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 |
|---|
| 70377-102-11 | 70377010211 | 30 TABLET in 1 BOTTLE (70377-102-11) | 30 tablet | 2021-03-15 | 0000-00-00 | No | No | Current |