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NDC 63629-1067-04 SPIRONOLACTONE 50 mg/1 Details
SPIRONOLACTONE 50 mg/1
SPIRONOLACTONE is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is SPIRONOLACTONE.
Product Information
NDC | 63629-1067 |
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Product ID | 63629-1067_df634fb8-5504-487a-8bae-b17dd0c82d16 |
Associated GPIs | 37500020000310 |
GCN Sequence Number | 006818 |
GCN Sequence Number Description | spironolactone TABLET 50 MG ORAL |
HIC3 | R1H |
HIC3 Description | POTASSIUM SPARING DIURETICS |
GCN | 27692 |
HICL Sequence Number | 002901 |
HICL Sequence Number Description | SPIRONOLACTONE |
Brand/Generic | Generic |
Proprietary Name | SPIRONOLACTONE |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | SPIRONOLACTONE |
Product Type | HUMAN PRESCRIPTION DRUG |
Dosage Form | TABLET, FILM COATED |
Route | ORAL |
Active Ingredient Strength | 50 |
Active Ingredient Units | mg/1 |
Substance Name | SPIRONOLACTONE |
Labeler Name | Bryant Ranch Prepack |
Pharmaceutical Class | Aldosterone Antagonist [EPC], Aldosterone Antagonists [MoA] |
DEA Schedule | n/a |
Marketing Category | ANDA |
Application Number | ANDA089424 |
Listing Certified Through | 2024-12-31 |
Package
NDC 63629-1067-04 (63629106704)
NDC Package Code | 63629-1067-4 |
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Billing NDC | 63629106704 |
Package | 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63629-1067-4) |
Marketing Start Date | 2022-10-26 |
NDC Exclude Flag | N |
Pricing Information | N/A |