Pill Identifier Information of tamsulosin hydrochloride 0.4 MG Modified Release Oral Capsule
Drug Information
tamsulosin hydrochloride 0.4 MG Modified Release Oral Capsule
| Imprint: | ZA;18;0;4mg |
| Shape: | C48336 |
| Color: | C48329;C48331 |
| Ingredients: | tamsulosin |
| Size: | 18.00 |
| Score: | 1 |
| Rxtty: | SY |
| Author: | Cadila Healthcare Limited |
| Inactive Ingredients: | D&C YELLOW NO. 10 / FD&C BLUE NO. 1 / FD&C RED NO. 40 / FD&C YELLOW NO. 6 / FERRIC OXIDE YELLOW / METHACRYLIC ACID / POLYSORBATE 80 / GELATIN / TALC / TITANIUM DIOXIDE / TRIACETIN / FERROSOFERRIC OXIDE / CELLULOSE, MICROCRYSTALLINE> |
Complete Information
- SPL UNCLASSIFIED SECTION
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
TAMSULOSIN HYDROCHLORIDEÂ
tamsulosin hydrochloride capsuleProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:65841-695 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TAMSULOSIN HYDROCHLORIDE (UNII: 11SV1951MR) (TAMSULOSIN - UNII:G3P28OML5I) TAMSULOSIN HYDROCHLORIDE 0.4 mg Inactive Ingredients Ingredient Name Strength D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  FD&C RED NO. 40 (UNII: WZB9127XOA)  FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  METHACRYLIC ACID (UNII: 1CS02G8656)  POLYSORBATE 80 (UNII: 6OZP39ZG8H)  GELATIN (UNII: 2G86QN327L)  TALC (UNII: 7SEV7J4R1U)  TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  TRIACETIN (UNII: XHX3C3X673)  FERROSOFERRIC OXIDE (UNII: XM0M87F357)  CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  Product Characteristics Color GREEN (GREEN) , ORANGE (PEACH) Score no score Shape CAPSULE (CAPSULE) Size 18mm Flavor Imprint Code ZA;18;0;4mg Contains     Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:65841-695-06 30 in 1 BOTTLE; Type 0: Not a Combination Product 04/27/2010 2 NDC:65841-695-14 60 in 1 BOTTLE; Type 0: Not a Combination Product 04/27/2010 3 NDC:65841-695-16 90 in 1 BOTTLE; Type 0: Not a Combination Product 04/27/2010 4 NDC:65841-695-01 100 in 1 BOTTLE; Type 0: Not a Combination Product 04/27/2010 5 NDC:65841-695-05 500 in 1 BOTTLE; Type 0: Not a Combination Product 04/27/2010 6 NDC:65841-695-10 1000 in 1 BOTTLE; Type 0: Not a Combination Product 04/27/2010 7 NDC:65841-695-77 10 in 1 CARTON 04/27/2010 7 10 in 1 BLISTER PACK; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA078225 04/27/2010 Labeler - Zydus Lifesciences Limited (918596198) Registrant - Zydus Lifesciences Limited (918596198) Establishment Name Address ID/FEI Business Operations Zydus Lifesciences Limited 918596198 ANALYSIS(65841-695) , MANUFACTURE(65841-695)
