Pill Identifier Imipramine Hydrochloride - NDC 0781-1764
Imipramine Hydrochloride
Product Code 0781-1764
Imipramine Hydrochloride by Sandoz Inc is a brow rou tablet film coated about 6 mm in size, imprinted with gg;47. The product is a human prescription drug with active ingredient(s) imipramine hydrochloride.
Imipramine Hydrochloride
Active Ingredient(s): Imipramine Hydrochloride
Inactive Ingredient(s):
- STARCH, CORN
- D&C YELLOW NO. 10
- FD&C BLUE NO. 2
- FD&C RED NO. 40
- HYDROXYPROPYL CELLULOSE (1600000 WAMW)
- HYPROMELLOSE, UNSPECIFIED
- ANHYDROUS LACTOSE
- MAGNESIUM STEARATE
- POLYETHYLENE GLYCOL, UNSPECIFIED
- POVIDONE, UNSPECIFIED
- TITANIUM DIOXIDE
Sandoz Inc
Product Type: Human Prescription Drug
Dosage Form: Tablet, Film Coated
- Brown (C48332)
Product Packages
NDC Package Code | Package Description |
---|---|
0781-1764-01 | 100 TABLET, FILM COATED in 1 BOTTLE |
0781-1764-10 | 1000 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.