Labetalol Hydrochloride
- Product NDC
- 68001-700
- 11-digit product format
- 680010700
- Labeler code
- 68001
- Product ID
- 68001-700_50c0ec04-5ccb-1979-e063-6294a90a4d74
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Labetalol Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- BluePoint Laboratories
- Application
- ANDA074787
- Marketing category
- ANDA
- Marketing start
- 2026-03-15
- Substance
- LABETALOL HYDROCHLORIDE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- 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 | 100 mg/1 |
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 |
|---|
| 68001-700-00 | Labetalol Hydrochloride | 100 in 1 BOTTLE | TABLET | 100 | | 2 |
| 68001-700-03 | Labetalol Hydrochloride | 500 in 1 BOTTLE | TABLET | 500 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 68001-700-00 | 68001070000 | 100 TABLET in 1 BOTTLE (68001-700-00) | 100 tablet | 2026-03-15 | No | No | Historical |
| 68001-700-03 | 68001070003 | 500 in 1 BOTTLE | | | | | Historical |