FDA Label for Ropinirole Hydrochloride
View Indications, Usage & Precautions
Ropinirole Hydrochloride Product Label
The following document was submitted to the FDA by the labeler of this product Zydus Lifesciences Limited. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Package Label.Principal Display Panel
NDC 65841-712-01 in bottle of 100 tablets
Ropinirole Hydrochloride Tablets, 0.25 mg
100 tablets
NDC 65841-713-01 in bottle of 100 tablets
Ropinirole Hydrochloride Tablets, 0.5 mg
100 tablets
NDC 65841-714-01 in bottle of 100 tablets
Ropinirole Hydrochloride Tablets, 1 mg
100 tablets
NDC 65841-715-01in bottle of 100 tablets
Ropinirole Hydrochloride Tablets, 2 mg
100 tablets
NDC 65841-716-01 in bottle of 100 tablets
Ropinirole Hydrochloride Tablets, 3 mg
100 tablets
NDC 65841-717-01 in bottle of 100 tablets
Ropinirole Hydrochloride Tablets, 4 mg
100 tablets
NDC 65841-718-01 in bottle of 100 tablets
Ropinirole Hydrochloride Tablets, 5 mg
100 tablets
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