Pill Identifier Labetalol Hydrochloride - NDC 70771-1163
Labetalol Hydrochloride
Product Code 70771-1163
Labetalol Hydrochloride by Cadila Healthcare Limited is a yellow rou tablet film coated about 8 mm in size, imprinted with 7;98. The product is a human prescription drug with active ingredient(s) labetalol hydrochloride.
Labetalol Hydrochloride
Active Ingredient(s): Labetalol Hydrochloride
Inactive Ingredient(s):
- ALUMINUM OXIDE
- D&C YELLOW NO. 10
- FERRIC OXIDE RED
- FERRIC OXIDE YELLOW
- HYPROMELLOSES
- LACTOSE MONOHYDRATE
- MAGNESIUM STEARATE
- POLYETHYLENE GLYCOL, UNSPECIFIED
- SODIUM STARCH GLYCOLATE TYPE A POTATO
- STARCH, CORN
- TALC
- TITANIUM DIOXIDE
Cadila Healthcare Limited
Product Type: Human Prescription Drug
Dosage Form: Tablet, Film Coated
- Yellow (C48330)
Product Packages
NDC Package Code | Package Description |
---|---|
70771-1163-1 | 100 TABLET, FILM COATED in 1 BOTTLE |
70771-1163-3 | 30 TABLET, FILM COATED in 1 BOTTLE |
70771-1163-5 | 500 TABLET, FILM COATED in 1 BOTTLE |
70771-1163-9 | 90 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.