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ENTSOL
ENTSOL - 10337-311-10 - (Sodium Chloride)
Drug Information of ENTSOL
| Product NDC: | 10337-311 |
| Proprietary Name: | ENTSOL |
| Non Proprietary Name: | Sodium Chloride |
| Active Ingredient(s): | 30 mg/mL & nbsp; Sodium Chloride |
| Administration Route(s): | NASAL |
| Dosage Form(s): | SPRAY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ENTSOL
| Product NDC: | 10337-311 |
| Labeler Name: | PharmaDerm, A division of Fougera Pharmaceuticals Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20000901 |
Package Information of ENTSOL
| Package NDC: | 10337-311-10 |
| Package Description: | 1 BOTTLE, SPRAY in 1 CARTON (10337-311-10) > 100 mL in 1 BOTTLE, SPRAY |
NDC Information of ENTSOL
| NDC Code | 10337-311-10 |
| Proprietary Name | ENTSOL |
| Package Description | 1 BOTTLE, SPRAY in 1 CARTON (10337-311-10) > 100 mL in 1 BOTTLE, SPRAY |
| Product NDC | 10337-311 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Sodium Chloride |
| Dosage Form Name | SPRAY |
| Route Name | NASAL |
| Start Marketing Date | 20000901 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | PharmaDerm, A division of Fougera Pharmaceuticals Inc. |
| Substance Name | SODIUM CHLORIDE |
| Strength Number | 30 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
