Heparin Sodium
- Product NDC
- 71288-422
- 11-digit product format
- 712880422
- Labeler code
- 71288
- Product ID
- 71288-422_62adb621-cc86-4702-8ba2-0fabedf075f4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Heparin Sodium
- Dosage form
- INJECTION
- Route
- INTRAVENOUS; SUBCUTANEOUS
- Labeler
- Meitheal Pharmaceuticals Inc.
- Application
- ANDA211007
- Marketing category
- ANDA
- Marketing start
- 2019-06-15
- Marketing end
- 0000-00-00
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71288-422 | HEPARIN SODIUM INJECTION [MEITHEAL PHARMACEUTICALS INC.] | 2 | Legacy NDC | 20211124_b6212d9b-d82b-46ea-9ba1-5410d04e0816.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71288-422-96 | 71288042296 | 25 VIAL, SINGLE-DOSE in 1 CARTON (71288-422-96) > 1 mL in 1 VIAL, SINGLE-DOSE (71288-422-95) | 2019-06-15 | 0000-00-00 | No | No | Current |