NOREPINEPHRINE BITARTRATE
- Product NDC
- 42023-247
- 11-digit product format
- 420230247
- Labeler code
- 42023
- Product ID
- 42023-247_88d4fb55-561d-486a-b061-f7cc17b45e33
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Norepinephrine in Sodium Chloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Par Pharmaceutical, Inc.
- Application
- NDA214628
- Marketing category
- NDA
- Marketing start
- 2023-01-04
- Marketing end
- 0000-00-00
- Substance
- NOREPINEPHRINE BITARTRATE
- Active strength
- 16 mg/250mL
- Pharmacologic classes
- Catecholamine [EPC], Catecholamines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 42023-247-10 | NOREPINEPHRINE BITARTRATE | 10 in 1 CARTON | INJECTION, SOLUTION | 10 | | 1 |
| 42023-247-10 | NOREPINEPHRINE BITARTRATE | 250 mL in 1 BAG | INJECTION, SOLUTION | 250 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 42023-247 | NOREPINEPHRINE BITARTRATE (NOREPINEPHRINE IN SODIUM CHLORIDE) INJECTION, SOLUTION NOREPINEPHRINE BITARTRATE (NOREPINEPHRINE IN SODIUM CHLORIDE) INJECTION, SOLUTION NOREPINEPHRINE BITARTRATE (NOREPINEPHRINE IN SODIUM CHLORIDE) INJECTION, SOLUTION [PAR PHARMACEUTICAL, INC.] | 1 | Legacy NDC, 2 package rows | 20230105_1f112215-cef7-46a0-b838-ba0542a99d2c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 42023-247-10 | 42023024710 | 10 BAG in 1 CARTON (42023-247-10) > 250 mL in 1 BAG | 10 bag | 2023-01-04 | 0000-00-00 | No | No | Current |