Propranolol hydrochloride capsule, extended release

Ingredients and appearance - Product information

Propranolol hydrochloride capsule, extended release- Propranolol hydrochloride

Product information

Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC: 49349-278
Route of Administration Oral

Active Ingredient/Active Moiety

Ingredient Name Strength
Propranolol hydrochloride ( UNII: F8A3652H1V)( Propranolol - UNII: 9Y8NXQ24VQ ) 60 mgin 1

Inactive Ingredients

Ingredient Name Code
Ethylcelluloses ( UNII: 7Z8S9VYZ4B)
Gelatin ( UNII: 2G86QN327L)
Hydroxypropyl cellulose ( UNII: RFW2ET671P)
Povidone ( UNII: FZ989GH94E)
D&c yellow no. 10 ( UNII: 35SW5USQ3G)
Talc ( UNII: 7SEV7J4R1U)
Titanium dioxide ( UNII: 15FIX9V2JP)
Fd&c blue no. 1 ( UNII: H3R47K3TBD)
Fd&c blue no. 2 ( UNII: L06K8R7DQK)
Fd&c red no. 40 ( UNII: WZB9127XOA)
Propylene glycol ( UNII: 6DC9Q167V3)

Product Characteristics

Color yellow Score 1
Shape CAPSULE (CAPSULE, EXTENDED RELEASE) Imprint Code 2778
Size 16 mm

Packaging

# Item Code Package Description Marketing Start Date
1 NDC: 49349-278-02 30 in 1 BLISTER PACK 2011/06/03

Marketing Information

Marketing Category Application Number or Monograph Citation Territorial Authority Marketing Start Date
ANDA ANDA078494 USA 2011/06/03

Labeler - REMEDYREPACK INC.( 829572556)