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NDC 59390-0183-13 Altachlore Sodium Chloride Hypertonicity 50 mg/mL Details
Altachlore Sodium Chloride Hypertonicity 50 mg/mL
Altachlore Sodium Chloride Hypertonicity is a OPHTHALMIC SOLUTION/ DROPS in the HUMAN OTC DRUG category. It is labeled and distributed by Altaire Pharmaceuticals Inc.. The primary component is SODIUM CHLORIDE.
Product Information
| NDC | 59390-0183 |
|---|---|
| Product ID | 59390-183_0c0e9c0d-61f5-e63b-e063-6294a90ac0d9 |
| Associated GPIs | 86804030102005 |
| GCN Sequence Number | 007739 |
| GCN Sequence Number Description | sodium chloride DROPS 5 % OPHTHALMIC |
| HIC3 | Q6A |
| HIC3 Description | OPHTHALMIC PREPARATIONS, MISCELLANEOUS |
| GCN | 31923 |
| HICL Sequence Number | 003389 |
| HICL Sequence Number Description | SODIUM CHLORIDE |
| Brand/Generic | Generic |
| Proprietary Name | Altachlore Sodium Chloride Hypertonicity |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Sodium Chloride |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | SOLUTION/ DROPS |
| Route | OPHTHALMIC |
| Active Ingredient Strength | 50 |
| Active Ingredient Units | mg/mL |
| Substance Name | SODIUM CHLORIDE |
| Labeler Name | Altaire Pharmaceuticals Inc. |
| Pharmaceutical Class | Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC] |
| DEA Schedule | n/a |
| Marketing Category | OTC MONOGRAPH DRUG |
| Application Number | M018 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 59390-0183-13 (59390018313)
| NDC Package Code | 59390-183-13 |
|---|---|
| Billing NDC | 59390018313 |
| Package | 1 BOTTLE, DROPPER in 1 CARTON (59390-183-13) / 15 mL in 1 BOTTLE, DROPPER |
| Marketing Start Date | 2002-09-24 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |