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Lacrisert
Lacrisert - 25010-805-68 - (hydroxypropyl cellulose)
Drug Information of Lacrisert
| Product NDC: | 25010-805 |
| Proprietary Name: | Lacrisert |
| Non Proprietary Name: | hydroxypropyl cellulose |
| Active Ingredient(s): | 5 mg/1 & nbsp; hydroxypropyl cellulose |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | PELLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Lacrisert
| Product NDC: | 25010-805 |
| Labeler Name: | Aton Pharma, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018771 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19810601 |
Package Information of Lacrisert
| Package NDC: | 25010-805-68 |
| Package Description: | 60 BLISTER PACK in 1 CARTON (25010-805-68) > 1 PELLET in 1 BLISTER PACK |
NDC Information of Lacrisert
| NDC Code | 25010-805-68 |
| Proprietary Name | Lacrisert |
| Package Description | 60 BLISTER PACK in 1 CARTON (25010-805-68) > 1 PELLET in 1 BLISTER PACK |
| Product NDC | 25010-805 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | hydroxypropyl cellulose |
| Dosage Form Name | PELLET |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19810601 |
| Marketing Category Name | NDA |
| Labeler Name | Aton Pharma, Inc. |
| Substance Name | HYDROXYPROPYL CELLULOSE |
| Strength Number | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Demulcent [EPC],Demulcent Activity [MoA] |
