Aminocaproic acid
- Product NDC
- 69539-161
- 11-digit product format
- 695390161
- Labeler code
- 69539
- Product ID
- 69539-161_60c079cb-5b45-4217-be17-5eb963af98e4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Aminocaproic acid
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- MSN LABORATORIES PRIVATE LIMITED
- Application
- ANDA212938
- Marketing category
- ANDA
- Marketing start
- 2020-11-09
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69539-161-30 | 69539016130 | 30 TABLET in 1 BOTTLE (69539-161-30) | 30 tablet | 2020-11-09 | 0000-00-00 | No | No | Current |