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Equaline Allergy relief
Equaline Allergy relief - 41163-311-65 - (Loratadine)
Drug Information of Equaline Allergy relief
| Product NDC: | 41163-311 |
| Proprietary Name: | Equaline Allergy relief |
| Non Proprietary Name: | Loratadine |
| Active Ingredient(s): | 10 mg/1 & nbsp; Loratadine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, ORALLY DISINTEGRATING |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Equaline Allergy relief
| Product NDC: | 41163-311 |
| Labeler Name: | Supervalu Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA075990 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20040805 |
Package Information of Equaline Allergy relief
| Package NDC: | 41163-311-65 |
| Package Description: | 3 BLISTER PACK in 1 CARTON (41163-311-65) > 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK |
NDC Information of Equaline Allergy relief
| NDC Code | 41163-311-65 |
| Proprietary Name | Equaline Allergy relief |
| Package Description | 3 BLISTER PACK in 1 CARTON (41163-311-65) > 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK |
| Product NDC | 41163-311 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Loratadine |
| Dosage Form Name | TABLET, ORALLY DISINTEGRATING |
| Route Name | ORAL |
| Start Marketing Date | 20040805 |
| Marketing Category Name | ANDA |
| Labeler Name | Supervalu Inc |
| Substance Name | LORATADINE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
