Pill Identifier Minocycline Hydrochloride - NDC 65862-885
Minocycline Hydrochloride
Product Code 65862-885
Minocycline Hydrochloride by Aurobindo Pharma Limited is a purple capsule tablet film coated extended release about 14 mm in size, imprinted with k;8. The product is a human prescription drug with active ingredient(s) minocycline hydrochloride.
Minocycline Hydrochloride
Active Ingredient(s): Minocycline Hydrochloride
Inactive Ingredient(s):
- SILICON DIOXIDE
- HYPROMELLOSE 2208 (4000 MPA.S)
- HYPROMELLOSE 2910 (15 MPA.S)
- HYPROMELLOSE 2910 (6 MPA.S)
- LACTOSE MONOHYDRATE
- MAGNESIUM STEARATE
- TITANIUM DIOXIDE
- TRIACETIN
- D&C RED NO. 27
- FD&C BLUE NO. 1
- POLYETHYLENE GLYCOL 3350
Aurobindo Pharma Limited
Product Type: Human Prescription Drug
Dosage Form: Tablet, Film Coated, Extended Release
- Purple (C48327)
Product Packages
NDC Package Code | Package Description |
---|---|
65862-885-01 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE |
65862-885-05 | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE |
65862-885-30 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE |
65862-885-99 | 1000 TABLET, FILM COATED, 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.