Aminocaproic acid
- Product NDC
- 60219-1637
- 11-digit product format
- 602191637
- Labeler code
- 60219
- Product ID
- 60219-1637_c69d729f-a296-42d7-a23e-517383f47d29
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Aminocaproic acid
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Amneal Pharmaceuticals NY LLC
- Application
- ANDA212492
- Marketing category
- ANDA
- Marketing start
- 2019-11-30
- Marketing end
- 0000-00-00
- Substance
- AMINOCAPROIC ACID
- Active strength
- 500 mg/1
- Pharmacologic classes
- Antifibrinolytic Agent [EPC],Decreased Fibrinolysis [PE]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 60219-1637-3 | Aminocaproic acid | 30 in 1 BOTTLE, PLASTIC | TABLET | 30 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60219-1637 | AMINOCAPROIC ACID TABLET [AMNEAL PHARMACEUTICALS NY LLC] | 5 | Legacy NDC, 1 package rows | 20200102_bc0267a5-15c9-4323-8cb9-44517bf87152.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 |
|---|
| 60219-1637-3 | 60219163703 | 30 TABLET in 1 BOTTLE, PLASTIC (60219-1637-3) | 30 tablet | 2019-11-30 | 0000-00-00 | No | No | Current |