Pill Identifier Venlafaxine Hydrochloride - NDC 16714-904
Venlafaxine Hydrochloride
Product Code 16714-904
Venlafaxine Hydrochloride by Northstar Rxllc is a pink and white rou tablet extended release about 8 mm in size, imprinted with 759. The product is a human prescription drug with active ingredient(s) venlafaxine hydrochloride.
Venlafaxine Hydrochloride
Active Ingredient(s): Venlafaxine Hydrochloride
Inactive Ingredient(s):
- HYPROMELLOSE 2208 (4000 MPA.S)
- POVIDONE K30
- LACTOSE MONOHYDRATE
- METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A
- TALC
- MAGNESIUM STEARATE
- MICROCRYSTALLINE CELLULOSE
- CROSPOVIDONE (15 MPA.S AT 5%)
- SILICON DIOXIDE
- SODIUM LAURYL SULFATE
- FD&C RED NO. 40
- MANNITOL
- DIBUTYL SEBACATE
- TRIETHYL CITRATE
- POLYSORBATE 20
- POLYETHYLENE GLYCOL 3350
- POLYSORBATE 80
- POLYVINYL ALCOHOL, UNSPECIFIED
Northstar Rxllc
Product Type: Human Prescription Drug
Dosage Form: Tablet, Extended Release
- Pink (C48328)
- White (C48325)
Product Packages
NDC Package Code | Package Description |
---|---|
16714-904-01 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE |
16714-904-02 | 90 TABLET, EXTENDED RELEASE 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.