Pill Identifier Information of amlodipine (as amlodipine besylate) 10 MG Oral Tablet
Drug Information
amlodipine (as amlodipine besylate) 10 MG Oral Tablet
| Imprint: | Z;5 |
| Shape: | C48348 |
| Color: | C48325 |
| Ingredients: | Amlodipine |
| Size: | 8.00 |
| Score: | 1 |
| Rxtty: | SY |
| Author: | Cadila Healthcare Limited |
| Inactive Ingredients: | MAGNESIUM STEARATE / SODIUM STARCH GLYCOLATE TYPE A POTATO / SILICON DIOXIDE / CELLULOSE, MICROCRYSTALLINE> |
Complete Information
- SPL UNCLASSIFIED SECTION
- SPL MEDGUIDE
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
AMLODIPINE BESYLATEÂ
amlodipine besylate tabletProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:65841-620 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMLODIPINE BESYLATE (UNII: 864V2Q084H) (AMLODIPINE - UNII:1J444QC288) AMLODIPINE 2.5 mg Inactive Ingredients Ingredient Name Strength MAGNESIUM STEARATE (UNII: 70097M6I30)  SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  Product Characteristics Color WHITE (WHITE TO OFF-WHITE) Score no score Shape ROUND (ROUND) Size 4mm Flavor Imprint Code Z;7 Contains     Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:65841-620-16 90 in 1 BOTTLE; Type 0: Not a Combination Product 09/21/2007 2 NDC:65841-620-01 100 in 1 BOTTLE; Type 0: Not a Combination Product 09/21/2007 3 NDC:65841-620-05 500 in 1 BOTTLE; Type 0: Not a Combination Product 09/21/2007 4 NDC:65841-620-77 10 in 1 CARTON 09/21/2007 4 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 ANDA078226 09/21/2007 AMLODIPINE BESYLATEÂ
amlodipine besylate tabletProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:65841-621 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMLODIPINE BESYLATE (UNII: 864V2Q084H) (AMLODIPINE - UNII:1J444QC288) AMLODIPINE 5 mg Inactive Ingredients Ingredient Name Strength MAGNESIUM STEARATE (UNII: 70097M6I30)  SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  Product Characteristics Color WHITE (WHITE TO OFF-WHITE) Score no score Shape ROUND (ROUND) Size 6mm Flavor Imprint Code Z;3 Contains     Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:65841-621-16 90 in 1 BOTTLE; Type 0: Not a Combination Product 09/21/2007 2 NDC:65841-621-01 100 in 1 BOTTLE; Type 0: Not a Combination Product 09/21/2007 3 NDC:65841-621-05 500 in 1 BOTTLE; Type 0: Not a Combination Product 09/21/2007 4 NDC:65841-621-77 10 in 1 CARTON 09/21/2007 4 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 ANDA078226 09/21/2007 AMLODIPINE BESYLATEÂ
amlodipine besylate tabletProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:65841-622 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMLODIPINE BESYLATE (UNII: 864V2Q084H) (AMLODIPINE - UNII:1J444QC288) AMLODIPINE 10 mg Inactive Ingredients Ingredient Name Strength MAGNESIUM STEARATE (UNII: 70097M6I30)  SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  Product Characteristics Color WHITE (WHITE TO OFF-WHITE) Score no score Shape ROUND (ROUND) Size 8mm Flavor Imprint Code Z;5 Contains     Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:65841-622-16 90 in 1 BOTTLE; Type 0: Not a Combination Product 09/21/2007 2 NDC:65841-622-01 100 in 1 BOTTLE; Type 0: Not a Combination Product 09/21/2007 3 NDC:65841-622-05 500 in 1 BOTTLE; Type 0: Not a Combination Product 09/21/2007 4 NDC:65841-622-77 10 in 1 CARTON 09/21/2007 4 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 ANDA078226 09/21/2007 Labeler - Zydus Lifesciences Limited (918596198) Registrant - Zydus Lifesciences Limited (918596198) Establishment Name Address ID/FEI Business Operations Zydus Lifesciences Limited 677605858 ANALYSIS(65841-620, 65841-621, 65841-622) , MANUFACTURE(65841-620, 65841-621, 65841-622) Establishment Name Address ID/FEI Business Operations Zydus Lifesciences Limited 918596198 ANALYSIS(65841-620, 65841-621, 65841-622) , MANUFACTURE(65841-620, 65841-621, 65841-622)
