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NDC 53002-1623-00 CHLORTHALIDONE 25 mg/1 Details
CHLORTHALIDONE 25 mg/1
CHLORTHALIDONE is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by RPK Pharmaceuticals, Inc.. The primary component is CHLORTHALIDONE.
MedlinePlus Drug Summary
Chlorthalidone, a 'water pill,' is used to treat high blood pressure and fluid retention caused by various conditions, including heart disease. It causes the kidneys to get rid of unneeded water and salt from the body into the urine. This medicine is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
Related Packages: 53002-1623-00Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Chlorthalidone
Product Information
NDC | 53002-1623 |
---|---|
Product ID | 53002-1623_124cc589-0fff-45f1-9ef7-70917b58e149 |
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 | CHLORTHALIDONE |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | CHLORTHALIDONE |
Product Type | HUMAN PRESCRIPTION DRUG |
Dosage Form | TABLET |
Route | ORAL |
Active Ingredient Strength | 25 |
Active Ingredient Units | mg/1 |
Substance Name | CHLORTHALIDONE |
Labeler Name | RPK Pharmaceuticals, Inc. |
Pharmaceutical Class | Increased Diuresis [PE], Thiazide-like Diuretic [EPC] |
DEA Schedule | n/a |
Marketing Category | ANDA |
Application Number | ANDA206904 |
Listing Certified Through | 2024-12-31 |
Package
NDC 53002-1623-00 (53002162300)
NDC Package Code | 53002-1623-0 |
---|---|
Billing NDC | 53002162300 |
Package | 100 TABLET in 1 BOTTLE (53002-1623-0) |
Marketing Start Date | 2017-09-01 |
NDC Exclude Flag | N |
Pricing Information | N/A |