Search by Drug Name or NDC
NDC 62135-0340-53 Sodium Polystyrene Sulfonate 4.1 meq/g Details
Sodium Polystyrene Sulfonate 4.1 meq/g
Sodium Polystyrene Sulfonate is a ORAL; RECTAL POWDER, FOR SUSPENSION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Chartwell RX, LLC. The primary component is SODIUM POLYSTYRENE SULFONATE.
Product Information
NDC | 62135-0340 |
---|---|
Product ID | 62135-340_06fcec70-ae79-a194-e063-6394a90a6ffa |
Associated GPIs | |
GCN Sequence Number | 001194 |
GCN Sequence Number Description | sodium polystyrene sulfonate POWDER ORAL |
HIC3 | C1A |
HIC3 Description | ELECTROLYTE DEPLETERS |
GCN | 02890 |
HICL Sequence Number | 013209 |
HICL Sequence Number Description | SODIUM POLYSTYRENE SULFONATE |
Brand/Generic | Generic |
Proprietary Name | Sodium Polystyrene Sulfonate |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | Sodium Polystyrene Sulfonate |
Product Type | HUMAN PRESCRIPTION DRUG |
Dosage Form | POWDER, FOR SUSPENSION |
Route | ORAL; RECTAL |
Active Ingredient Strength | 4.1 |
Active Ingredient Units | meq/g |
Substance Name | SODIUM POLYSTYRENE SULFONATE |
Labeler Name | Chartwell RX, LLC |
Pharmaceutical Class | n/a |
DEA Schedule | n/a |
Marketing Category | ANDA |
Application Number | ANDA206815 |
Listing Certified Through | 2024-12-31 |
Package
NDC 62135-0340-53 (62135034053)
NDC Package Code | 62135-340-53 |
---|---|
Billing NDC | 62135034053 |
Package | 453.6 g in 1 BOTTLE (62135-340-53) |
Marketing Start Date | 2022-07-20 |
NDC Exclude Flag | N |
Pricing Information | N/A |