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NDC 16714-0637-01 Spironolactone 25 mg/1 Details
Spironolactone 25 mg/1
Spironolactone is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by NorthStar RxLLC. The primary component is SPIRONOLACTONE.
Product Information
| NDC | 16714-0637 |
|---|---|
| Product ID | 16714-637_ee4b013a-434e-77ae-e053-2a95a90a1c6d |
| Associated GPIs | |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| 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 | 25 |
| Active Ingredient Units | mg/1 |
| Substance Name | SPIRONOLACTONE |
| Labeler Name | NorthStar RxLLC |
| Pharmaceutical Class | Aldosterone Antagonist [EPC], Aldosterone Antagonists [MoA] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA203512 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 16714-0637-01 (16714063701)
| NDC Package Code | 16714-637-01 |
|---|---|
| Billing NDC | 16714063701 |
| Package | 100 TABLET, FILM COATED in 1 BOTTLE (16714-637-01) |
| Marketing Start Date | 2022-11-18 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |