Labetalol Hydrochloride
- Product NDC
- 55154-4747
- 11-digit product format
- 551544747
- Labeler code
- 55154
- Product ID
- 55154-4747_ae113f45-ad3e-4bd8-9119-b68d305b9af9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Labetalol Hydrochloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Cardinal Health 107, LLC
- Application
- ANDA075239
- Marketing category
- ANDA
- Marketing start
- 1999-11-29
- Substance
- LABETALOL HYDROCHLORIDE
- Active strength
- 5 mg/mL
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Labetalol Hydrochloride
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| LABETALOL HYDROCHLORIDE | 5 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 1GEV3BAW9J |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 55154-4747-5 | Labetalol Hydrochloride | 4 mL in 1 CARTRIDGE | INJECTION, SOLUTION | 4 | | 12 |
| 55154-4747-5 | Labetalol Hydrochloride | 5 in 1 BAG | INJECTION, SOLUTION | 5 | | 12 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| LABETALOL HYDROCHLORIDE | ACTIVE INGREDIENT | 1GEV3BAW9J | LABETALOL HYDROCHLORIDE INJECTION, SOLUTION [CARDINAL HEALTH] | 1 | |
| LABETALOL | ACTIVE MOIETY | R5H8897N95 | LABETALOL HYDROCHLORIDE INJECTION, SOLUTION [CARDINAL HEALTH] | 1 | |
| ANHYDROUS DEXTROSE | INACTIVE INGREDIENT | 5SL0G7R0OK | LABETALOL HYDROCHLORIDE INJECTION, SOLUTION [CARDINAL HEALTH] | 1 | |
| CITRIC ACID MONOHYDRATE | INACTIVE INGREDIENT | 2968PHW8QP | LABETALOL HYDROCHLORIDE INJECTION, SOLUTION [CARDINAL HEALTH] | 1 | |
| EDETATE DISODIUM | INACTIVE INGREDIENT | 7FLD91C86K | LABETALOL HYDROCHLORIDE INJECTION, SOLUTION [CARDINAL HEALTH] | 1 | |
| METHYLPARABEN | INACTIVE INGREDIENT | A2I8C7HI9T | LABETALOL HYDROCHLORIDE INJECTION, SOLUTION [CARDINAL HEALTH] | 1 | |
| PROPYLPARABEN | INACTIVE INGREDIENT | Z8IX2SC1OH | LABETALOL HYDROCHLORIDE INJECTION, SOLUTION [CARDINAL HEALTH] | 1 | |
| SODIUM HYDROXIDE | INACTIVE INGREDIENT | 55X04QC32I | LABETALOL HYDROCHLORIDE INJECTION, SOLUTION [CARDINAL HEALTH] | 1 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 55154-4747 | LABETALOL HYDROCHLORIDE INJECTION, SOLUTION [CARDINAL HEALTH 107, LLC] | 11 | Current NDC, Legacy NDC, 2 package rows | 20240929_1b96ddc9-d0c3-488a-a113-66491fd3d899.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 |
|---|
| 55154-4747-5 | 55154474705 | 5 CARTRIDGE in 1 BAG (55154-4747-5) / 4 mL in 1 CARTRIDGE | 5 cartridge | 1999-11-29 | 0000-00-00 | No | No | Current |