AMICAR
- Product NDC
- 68151-3023
- 11-digit product format
- 681513023
- Labeler code
- 68151
- Product ID
- 68151-3023_d6835f27-90b9-4a4a-bb33-9d34ea1a88b1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Aminocaproic Acid
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Carilion Materials Management
- Application
- NDA015197
- Marketing category
- NDA
- Marketing start
- 2015-06-01
- 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
- 2019-12-31
- 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 |
|---|
| 68151-3023-1 | AMICAR | 1 in 1 BLISTER PACK | TABLET | 1 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68151-3023 | AMICAR (AMINOCAPROIC ACID) TABLET [CARILION MATERIALS MANAGEMENT] | 5 | Legacy NDC, 1 package rows | 20180817_05b08095-2acc-47ef-a426-b68c7d95de95.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 68151-3023-1 | 68151302301 | 1 in 1 BLISTER PACK | Historical |