METFORMIN HYDROCHLORIDE EXTENDED RELEASE (Page 2 of 2)

PRINCIPAL DISPLAY PANEL

DRUG: METFORMIN HYDROCHLORIDE EXTENDED RELEASE

GENERIC: METFORMIN HYDROCHLORIDE

DOSAGE: TABLET, EXTENDED RELEASE

ADMINSTRATION: ORAL

NDC: 70518-2480-0

COLOR: white

SHAPE: CAPSULE

SCORE: No score

SIZE: 19 mm

IMPRINT: 102

PACKAGING: 30 in 1 BLISTER PACK

ACTIVE INGREDIENT(S):

  • METFORMIN HYDROCHLORIDE 750mg in 1

INACTIVE INGREDIENT(S):

  • HYPROMELLOSE 2208 (100 MPA.S)
  • MAGNESIUM STEARATE
  • SILICON DIOXIDE
Remedy_Label
(click image for full-size original)
METFORMIN HYDROCHLORIDE EXTENDED RELEASE metformin hydrochloride tablet, extended release
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:70518-2480(NDC:49483-624)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
METFORMIN HYDROCHLORIDE (METFORMIN) METFORMIN HYDROCHLORIDE 750 mg
Inactive Ingredients
Ingredient Name Strength
HYPROMELLOSE 2208 (100 MPA.S)
SILICON DIOXIDE
MAGNESIUM STEARATE
Product Characteristics
Color white Score no score
Shape CAPSULE Size 19mm
Flavor Imprint Code 102
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:70518-2480-0 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA090295 12/12/2019
Labeler — REMEDYREPACK INC. (829572556)

Revised: 12/2019 REMEDYREPACK INC.

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