Aminocaproic Acid
- Product NDC
- 17478-769
- 11-digit product format
- 174780769
- Labeler code
- 17478
- Product ID
- 17478-769_44814e91-37c0-4652-8c2b-96a35e23c45b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Aminocaproic Acid
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Akorn Operating Company LLC
- Application
- NDA015197
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2019-03-12
- Marketing end
- 0000-00-00
- Substance
- AMINOCAPROIC ACID
- Active strength
- 1000 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 Product Concepts#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 17478-769 | AMINOCAPROIC ACID TABLET AMINOCAPROIC ACID SYRUP [AKORN OPERATING COMPANY LLC] | 3 | Legacy NDC | 20220707_f90e9443-78d3-4709-b6be-ee9aacef2afb.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 17478-769-30 | 17478076930 | 30 TABLET in 1 BOTTLE (17478-769-30) | 30 tablet | 2019-03-12 | 0000-00-00 | No | No | Current |