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NDC 62250-0660-23 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 Belcher Pharmaceuticals, LLC. The primary component is SODIUM POLYSTYRENE SULFONATE.
Product Information
| NDC | 62250-0660 |
|---|---|
| Product ID | 62250-660_06f95483-7080-8e4b-e063-6294a90a1992 |
| 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 | Belcher Pharmaceuticals, LLC |
| Pharmaceutical Class | n/a |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA205727 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 62250-0660-23 (62250066023)
| NDC Package Code | 62250-660-23 |
|---|---|
| Billing NDC | 62250066023 |
| Package | 454 g in 1 BOTTLE (62250-660-23) |
| Marketing Start Date | 2016-03-15 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |