AMINOCAPROIC ACID
- Product NDC
- 52584-346
- 11-digit product format
- 525840346
- Labeler code
- 52584
- Product ID
- 52584-346_3a5369e2-2255-45c2-a9a3-a4674863d0a3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- AMINOCAPROIC ACID
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- General Injectables and Vaccines, Inc.
- Application
- ANDA070010
- Marketing category
- ANDA
- Marketing start
- 2018-07-02
- Marketing end
- 0000-00-00
- Substance
- AMINOCAPROIC ACID
- Active strength
- 250 mg/mL
- Pharmacologic classes
- Antifibrinolytic Agent [EPC],Decreased Fibrinolysis [PE]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 52584-346-16 | 52584034616 | 1 VIAL, SINGLE-DOSE in 1 BAG (52584-346-16) > 20 mL in 1 VIAL, SINGLE-DOSE | 2018-07-02 | 0000-00-00 | No | No | Current |