Pill Identifier Bisoprolol Fumarate And Hydrochlorothiazide - NDC 42799-920
Bisoprolol Fumarate And Hydrochlorothiazide
Product Code 42799-920
Bisoprolol Fumarate And Hydrochlorothiazide by Edenbridge Pharmaceuticals Llc. is a yellow rou tablet film coated about 7 mm in size, imprinted with 920. The product is a human prescription drug with active ingredient(s) bisoprolol fumarate and hydrochlorothiazide.
Bisoprolol Fumarate And Hydrochlorothiazide
Active Ingredient(s): Bisoprolol Fumarate And Hydrochlorothiazide
Inactive Ingredient(s):
- CELLULOSE, MICROCRYSTALLINE
- ANHYDROUS LACTOSE
- STARCH, CORN
- CROSPOVIDONE
- STEARIC ACID
- HYPROMELLOSE 2910 (3 MPA.S)
- HYPROMELLOSE 2910 (6 MPA.S)
- TITANIUM DIOXIDE
- D&C YELLOW NO. 10
- POLYETHYLENE GLYCOL 400
- POLYSORBATE 80
- FD&C YELLOW NO. 6
Edenbridge Pharmaceuticals Llc.
Product Type: Human Prescription Drug
Dosage Form: Tablet, Film Coated
- Yellow (C48330)
Product Packages
NDC Package Code | Package Description |
---|---|
42799-920-01 | 100 TABLET, FILM COATED in 1 BOTTLE |
42799-920-02 | 500 TABLET, FILM COATED in 1 BOTTLE |
42799-920-30 | 30 TABLET, FILM COATED in 1 BOTTLE |
* 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.