Heparin Sodium
- Product NDC
- 0264-5705
- 11-digit product format
- 002645705
- Labeler code
- 0264
- Product ID
- 0264-5705_12d0886b-aa54-417e-a235-2dce060ea52d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Heparin Sodium
- Dosage form
- INJECTION
- Route
- INTRAVENOUS; SUBCUTANEOUS
- Labeler
- B. Braun Medical Inc.
- Application
- ANDA208827
- Marketing category
- ANDA
- Marketing start
- 2019-04-08
- Marketing end
- 0000-00-00
- Substance
- HEPARIN SODIUM
- Active strength
- 5000 [USP'U]/.5mL
- Pharmacologic classes
- Anti-coagulant [EPC], Heparin [CS], Unfractionated Heparin [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 0264-5705 | HEPARIN SODIUM INJECTION [B. BRAUN MEDICAL INC.] | 7 | Legacy NDC | 20221117_83c0c7c4-96ff-4e2d-85be-628bfd5ed771.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0264-5705-10 | 00264570510 | 10 BLISTER PACK in 1 CARTON (0264-5705-10) > 1 SYRINGE in 1 BLISTER PACK (0264-5705-05) > .5 mL in 1 SYRINGE | 10 blister pack | 2019-04-08 | 0000-00-00 | No | No | Current |