Pill Identifier Labetalol Hydrochloride - NDC 0591-0605
Labetalol Hydrochloride
Product Code 0591-0605
Labetalol Hydrochloride by Actavis Pharma, Inc. is a brow rou tablet film coated about 8 mm in size, imprinted with watson;605. The product is a human prescription drug with active ingredient(s) labetalol hydrochloride.
Labetalol Hydrochloride
Active Ingredient(s): Labetalol Hydrochloride
Inactive Ingredient(s):
- ANHYDROUS LACTOSE
- SILICON DIOXIDE
- CROSPOVIDONE
- HYPROMELLOSES
- MAGNESIUM STEARATE
- CELLULOSE, MICROCRYSTALLINE
- POLYETHYLENE GLYCOL, UNSPECIFIED
- POLYSORBATE 80
- STARCH, CORN
- WATER
- TITANIUM DIOXIDE
- FERRIC OXIDE RED
- FERRIC OXIDE YELLOW
Actavis Pharma, Inc.
Product Type: Human Prescription Drug
Dosage Form: Tablet, Film Coated
- Brown (C48332)
Product Packages
NDC Package Code | Package Description |
---|---|
0591-0605-00 | 64700 TABLET, FILM COATED in 1 BAG |
0591-0605-01 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC |
0591-0605-05 | 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC |
0591-0605-10 | 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC |
0591-0605-77 | 77664 TABLET, FILM COATED in 1 CONTAINER |
* Please review the disclaimer below.
Pill Identification data last updated on: December, 2018
This product uses publicly available data from the U.S. National Library of Medicine (NLM), National Institutes of Health, Department of Health and Human Services; NLM is not responsible for the product and does not endorse or recommend this or any other product. If this is an emergency, call 911 or the national Poison Help hotline at 1-800-222-1222. Most images are not part of the product labels and have not been verified by the labeler company. ALWAYS consult your physician or pharmacist with any medication-related questions.