Heparin Sodium
- Product NDC
- 87188-102
- 11-digit product format
- 871880102
- Labeler code
- 87188
- Product ID
- 87188-102_4deaa9b8-9a35-cefc-e063-6394a90a0aa9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Heparin Sodium
- Dosage form
- INJECTION
- Route
- INTRAVENOUS; SUBCUTANEOUS
- Labeler
- Plano Pharmaceuticals Inc.
- Application
- ANDA091682
- Marketing category
- ANDA
- Marketing start
- 2011-06-08
- Substance
- HEPARIN SODIUM
- Active strength
- 5000 [USP'U]/mL
- Pharmacologic classes
- Anti-coagulant [EPC], Heparin [CS], Unfractionated Heparin [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Heparin Sodium
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| HEPARIN SODIUM | 5000 [USP'U]/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | ZZ45AB24CA |
| Rxcui | 1361615 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 87188-102-01 | Heparin Sodium | 1 mL in 1 VIAL, MULTI-DOSE | INJECTION | 1 | | 1 |
| 87188-102-90 | Heparin Sodium | 25 in 1 CARTON | INJECTION | 25 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 87188-102-01 | 87188010201 | 1 mL in 1 VIAL, MULTI-DOSE | 1 ml | | | | Historical |
| 87188-102-90 | 87188010290 | 25 VIAL, MULTI-DOSE in 1 CARTON (87188-102-90) / 1 mL in 1 VIAL, MULTI-DOSE (87188-102-01) | | 2016-12-08 | No | No | Historical |