Aminocaproic Acid
- Product NDC
- 42799-054
- 11-digit product format
- 427990054
- Labeler code
- 42799
- Product ID
- 42799-054_c32edc1c-beb6-44eb-ac7d-f0b40ac42946
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Aminocaproic Acid
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Edenbridge Pharmaceuticals LLC.
- Application
- ANDA212110
- Marketing category
- ANDA
- Marketing start
- 2021-06-02
- 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
- 2022-12-31
- 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 |
|---|
| 42799-054-02 | 42799005402 | 30 TABLET in 1 BOTTLE (42799-054-02) | 30 tablet | 2021-06-02 | 0000-00-00 | No | No | Current |