Nortriptyline hydrochloride capsule

Ingredients and appearance - Product information

Nortriptyline hydrochloride capsule- Nortriptyline hydrochloride

Product information

Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC: 50436-0810
Route of Administration Oral

Active Ingredient/Active Moiety

Ingredient Name Strength
Nortriptyline hydrochloride ( UNII: 00FN6IH15D)( Nortriptyline - UNII: BL03SY4LXB ) 10 mgin 1

Inactive Ingredients

Ingredient Name Code
Starch, corn ( UNII: O8232NY3SJ)
D&c yellow no. 10 ( UNII: 35SW5USQ3G)
Fd&c blue no. 1 ( UNII: H3R47K3TBD)
Fd&c blue no. 2 ( UNII: L06K8R7DQK)
Fd&c red no. 40 ( UNII: WZB9127XOA)
Gelatin, unspecified ( UNII: 2G86QN327L)
Ferrosoferric oxide ( UNII: XM0M87F357)
Methylparaben ( UNII: A2I8C7HI9T)
Propylene glycol ( UNII: 6DC9Q167V3)
Propylparaben ( UNII: Z8IX2SC1OH)
Shellac ( UNII: 46N107B71O)
Dimethicone ( UNII: 92RU3N3Y1O)
Sodium lauryl sulfate ( UNII: 368GB5141J)
Titanium dioxide ( UNII: 15FIX9V2JP)
Fd&c yellow no. 6 ( UNII: H77VEI93A8)

Product Characteristics

Color ORANGE Imprint Code TEVA;10mg;0810
Score 1 Shape CAPSULE
Size 16 mm

Packaging

# Item Code Package Description Marketing Start Date
1 NDC: 50436-0810-1 30 in 1 BOTTLE 2017/07/05

Marketing Information

Marketing Category Application Number or Monograph Citation Territorial Authority Marketing Start Date
ANDA ANDA074132 USA 2017/07/05

Labeler - Unit Dose Services( 831995316)

Establishment

Name ID/FEI Business Operations
Unit Dose Services 831995316 REPACK( 50436-0810), RELABEL( 50436-0810)

Nortriptyline hydrochloride capsule