Label: RAMIPRIL capsule
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NDC Code(s):
65841-655-01,
65841-655-05,
65841-655-06,
65841-655-16, view more65841-655-30, 65841-656-01, 65841-656-05, 65841-656-06, 65841-656-16, 65841-656-30, 65841-657-01, 65841-657-05, 65841-657-06, 65841-657-16, 65841-657-30, 65841-658-01, 65841-658-05, 65841-658-06, 65841-658-16, 65841-658-30
- Packager: Zydus Lifesciences Limited
- Category: HUMAN PRESCRIPTION DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated July 31, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
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PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
NDC 65841-655-06 in bottle of 30 Capsules
Ramipril Capsules, 1.25 mg
Rx only
30 Capsules
NDC 65841-656-01 in bottle of 100 Capsules
Ramipril Capsules, 2.5 mg
Rx only
100 Capsules
NDC 65841-657-01 in bottle of 100 Capsules
Ramipril Capsules, 5 mg
Rx only
100 Capsules
NDC 65841-658-01 in bottle of 100 Capsules
Ramipril Capsules, 10 mg
Rx only
100 Capsules
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INGREDIENTS AND APPEARANCE
RAMIPRIL
ramipril capsuleProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:65841-655 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength RAMIPRIL (UNII: L35JN3I7SJ) (RAMIPRILAT - UNII:6N5U4QFC3G) RAMIPRIL 1.25 mg Inactive Ingredients Ingredient Name Strength FD&C RED NO. 40 (UNII: WZB9127XOA) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) FD&C YELLOW NO. 6 (UNII: H77VEI93A8) GELATIN (UNII: 2G86QN327L) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) STARCH, CORN (UNII: O8232NY3SJ) FERROSOFERRIC OXIDE (UNII: XM0M87F357) Product Characteristics Color WHITE (WHITE) , YELLOW (YELLOW) Score no score Shape CAPSULE (CAPSULE) Size 14mm Flavor Imprint Code ZA;43;1;25mg Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:65841-655-06 30 in 1 BOTTLE; Type 0: Not a Combination Product 11/20/2010 2 NDC:65841-655-16 90 in 1 BOTTLE; Type 0: Not a Combination Product 11/20/2010 3 NDC:65841-655-01 100 in 1 BOTTLE; Type 0: Not a Combination Product 11/20/2010 4 NDC:65841-655-05 500 in 1 BOTTLE; Type 0: Not a Combination Product 11/20/2010 5 NDC:65841-655-30 10 in 1 CARTON 11/20/2010 5 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 ANDA078832 11/20/2010 RAMIPRIL
ramipril capsuleProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:65841-656 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength RAMIPRIL (UNII: L35JN3I7SJ) (RAMIPRILAT - UNII:6N5U4QFC3G) RAMIPRIL 2.5 mg Inactive Ingredients Ingredient Name Strength D&C YELLOW NO. 10 (UNII: 35SW5USQ3G) FD&C RED NO. 40 (UNII: WZB9127XOA) GELATIN (UNII: 2G86QN327L) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) STARCH, CORN (UNII: O8232NY3SJ) FERROSOFERRIC OXIDE (UNII: XM0M87F357) Product Characteristics Color WHITE (WHITE) , ORANGE (ORANGE) Score no score Shape CAPSULE (CAPSULE) Size 14mm Flavor Imprint Code ZA;44;2;5mg Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:65841-656-06 30 in 1 BOTTLE; Type 0: Not a Combination Product 11/20/2010 2 NDC:65841-656-16 90 in 1 BOTTLE; Type 0: Not a Combination Product 11/20/2010 3 NDC:65841-656-01 100 in 1 BOTTLE; Type 0: Not a Combination Product 11/20/2010 4 NDC:65841-656-05 500 in 1 BOTTLE; Type 0: Not a Combination Product 11/20/2010 5 NDC:65841-656-30 10 in 1 CARTON 11/20/2010 5 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 ANDA078832 11/20/2010 RAMIPRIL
ramipril capsuleProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:65841-657 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength RAMIPRIL (UNII: L35JN3I7SJ) (RAMIPRILAT - UNII:6N5U4QFC3G) RAMIPRIL 5 mg Inactive Ingredients Ingredient Name Strength FD&C BLUE NO. 1 (UNII: H3R47K3TBD) FD&C RED NO. 40 (UNII: WZB9127XOA) FD&C YELLOW NO. 6 (UNII: H77VEI93A8) GELATIN (UNII: 2G86QN327L) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) STARCH, CORN (UNII: O8232NY3SJ) FERROSOFERRIC OXIDE (UNII: XM0M87F357) Product Characteristics Color WHITE (WHITE) , RED (RED) Score no score Shape CAPSULE (CAPSULE) Size 14mm Flavor Imprint Code ZA;45;5mg Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:65841-657-06 30 in 1 BOTTLE; Type 0: Not a Combination Product 11/20/2010 2 NDC:65841-657-16 90 in 1 BOTTLE; Type 0: Not a Combination Product 11/20/2010 3 NDC:65841-657-01 100 in 1 BOTTLE; Type 0: Not a Combination Product 11/20/2010 4 NDC:65841-657-05 500 in 1 BOTTLE; Type 0: Not a Combination Product 11/20/2010 5 NDC:65841-657-30 10 in 1 CARTON 11/20/2010 5 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 ANDA078832 11/20/2010 RAMIPRIL
ramipril capsuleProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:65841-658 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength RAMIPRIL (UNII: L35JN3I7SJ) (RAMIPRILAT - UNII:6N5U4QFC3G) RAMIPRIL 10 mg Inactive Ingredients Ingredient Name Strength D&C RED NO. 28 (UNII: 767IP0Y5NH) D&C YELLOW NO. 10 (UNII: 35SW5USQ3G) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) GELATIN (UNII: 2G86QN327L) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) STARCH, CORN (UNII: O8232NY3SJ) FERROSOFERRIC OXIDE (UNII: XM0M87F357) Product Characteristics Color WHITE (WHITE) , BLUE (BLUE) Score no score Shape CAPSULE (CAPSULE) Size 14mm Flavor Imprint Code ZA;46;10mg Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:65841-658-06 30 in 1 BOTTLE; Type 0: Not a Combination Product 11/20/2010 2 NDC:65841-658-16 90 in 1 BOTTLE; Type 0: Not a Combination Product 11/20/2010 3 NDC:65841-658-01 100 in 1 BOTTLE; Type 0: Not a Combination Product 11/20/2010 4 NDC:65841-658-05 500 in 1 BOTTLE; Type 0: Not a Combination Product 11/20/2010 5 NDC:65841-658-30 10 in 1 CARTON 11/20/2010 5 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 ANDA078832 11/20/2010 Labeler - Zydus Lifesciences Limited (918596198) Registrant - Zydus Lifesciences Limited (918596198) Establishment Name Address ID/FEI Business Operations Zydus Lifesciences Limited 918596198 ANALYSIS(65841-655, 65841-656, 65841-657, 65841-658) , MANUFACTURE(65841-655, 65841-656, 65841-657, 65841-658)