Ribavirinum by Hahnemann Laboratories, INC. RIBAVIRINUM pellet
Ribavirinum by
Drug Labeling and Warnings
Ribavirinum by is a Homeopathic medication manufactured, distributed, or labeled by Hahnemann Laboratories, INC.. Drug facts, warnings, and ingredients follow.
Drug Details [pdf]
- ACTIVE INGREDIENT
- DOSAGE FORMS & STRENGTHS
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- PREGNANCY OR BREAST FEEDING
- ASK DOCTOR
- KEEP OUT OF REACH OF CHILDREN
- INSTRUCTIONS FOR USE
- DOSAGE & ADMINISTRATION
- ROUTE, METHOD AND FREQUENCY OF ADMINISTRATION
- INACTIVE INGREDIENT
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
RIBAVIRINUM
ribavirinum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-4137 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength RIBAVIRIN (UNII: 49717AWG6K) (RIBAVIRIN - UNII:49717AWG6K) RIBAVIRIN 12 [hp_C] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) Product Characteristics Color white Score no score Shape ROUND Size 3mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 37662-4137-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 10/12/2023 2 NDC: 37662-4137-2 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 10/12/2023 3 NDC: 37662-4137-3 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 10/12/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 10/12/2023 RIBAVIRINUM
ribavirinum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-4138 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength RIBAVIRIN (UNII: 49717AWG6K) (RIBAVIRIN - UNII:49717AWG6K) RIBAVIRIN 30 [hp_C] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) Product Characteristics Color white Score no score Shape ROUND Size 3mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 37662-4138-1 80 in 1 VIAL, GLASS; Type 0: Not a Combination Product 10/12/2023 2 NDC: 37662-4138-2 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 10/12/2023 3 NDC: 37662-4138-3 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 10/12/2023 4 NDC: 37662-4138-4 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 10/12/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 10/12/2023 RIBAVIRINUM
ribavirinum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-4139 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength RIBAVIRIN (UNII: 49717AWG6K) (RIBAVIRIN - UNII:49717AWG6K) RIBAVIRIN 100 [hp_C] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) Product Characteristics Color white Score no score Shape ROUND Size 2mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 37662-4139-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 10/12/2023 2 NDC: 37662-4139-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 10/12/2023 3 NDC: 37662-4139-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 10/12/2023 4 NDC: 37662-4139-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 10/12/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 10/12/2023 RIBAVIRINUM
ribavirinum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-4140 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength RIBAVIRIN (UNII: 49717AWG6K) (RIBAVIRIN - UNII:49717AWG6K) RIBAVIRIN 200 [hp_C] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) Product Characteristics Color white Score no score Shape ROUND Size 2mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 37662-4140-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 10/12/2023 2 NDC: 37662-4140-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 10/12/2023 3 NDC: 37662-4140-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 10/12/2023 4 NDC: 37662-4140-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 10/12/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 10/12/2023 RIBAVIRINUM
ribavirinum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-4136 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength RIBAVIRIN (UNII: 49717AWG6K) (RIBAVIRIN - UNII:49717AWG6K) RIBAVIRIN 6 [hp_C] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) Product Characteristics Color white Score no score Shape ROUND Size 3mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 37662-4136-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 10/12/2023 2 NDC: 37662-4136-2 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 10/12/2023 3 NDC: 37662-4136-3 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 10/12/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 10/12/2023 RIBAVIRINUM
ribavirinum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-4142 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength RIBAVIRIN (UNII: 49717AWG6K) (RIBAVIRIN - UNII:49717AWG6K) RIBAVIRIN 1 [hp_M] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) Product Characteristics Color white Score no score Shape ROUND Size 2mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 37662-4142-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 10/12/2023 2 NDC: 37662-4142-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 10/12/2023 3 NDC: 37662-4142-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 10/12/2023 4 NDC: 37662-4142-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 10/12/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 10/12/2023 RIBAVIRINUM
ribavirinum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-4143 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength RIBAVIRIN (UNII: 49717AWG6K) (RIBAVIRIN - UNII:49717AWG6K) RIBAVIRIN 1 [hp_Q] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) Product Characteristics Color white Score no score Shape ROUND Size 1mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 37662-4143-1 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 10/12/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 10/12/2023 RIBAVIRINUM
ribavirinum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 37662-4141 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength RIBAVIRIN (UNII: 49717AWG6K) (RIBAVIRIN - UNII:49717AWG6K) RIBAVIRIN 500 [hp_C] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) Product Characteristics Color white Score no score Shape ROUND Size 2mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 37662-4141-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 10/12/2023 2 NDC: 37662-4141-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 10/12/2023 3 NDC: 37662-4141-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 10/12/2023 4 NDC: 37662-4141-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 10/12/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 10/12/2023 Labeler - Hahnemann Laboratories, INC. (147098081) Establishment Name Address ID/FEI Business Operations Hahnemann Laboratories, INC. 147098081 manufacture(37662-4136, 37662-4137, 37662-4138, 37662-4139, 37662-4140, 37662-4141, 37662-4142, 37662-4143)
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