Lacrisert is a Ophthalmic Insert in the Human Prescription Drug category. It is labeled and distributed by Bausch & Lomb Incorporated. The primary component is Hydroxypropyl Cellulose (1600000 Wamw).
| Product ID | 24208-800_0a58496a-ebf3-46df-a3d9-2cb096e5ff69 |
| NDC | 24208-800 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Lacrisert |
| Generic Name | Hydroxypropyl Cellulose |
| Dosage Form | Insert |
| Route of Administration | OPHTHALMIC |
| Marketing Start Date | 1981-06-01 |
| Marketing Category | NDA / NDA |
| Application Number | NDA018771 |
| Labeler Name | Bausch & Lomb Incorporated |
| Substance Name | HYDROXYPROPYL CELLULOSE (1600000 WAMW) |
| Active Ingredient Strength | 5 mg/1 |
| Pharm Classes | Demulcent [EPC],Demulcent Activity [MoA] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2021-12-31 |
| Marketing Start Date | 1981-06-01 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | NDA |
| Application Number | NDA018771 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1981-06-01 |
| Marketing Category | NDA |
| Application Number | NDA018771 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1981-06-01 |
| Ingredient | Strength |
|---|---|
| HYDROXYPROPYL CELLULOSE (TYPE H) | 5 mg/1 |
| SPL SET ID: | cc7a6a52-0b77-4df7-8403-dd21c1334f6c |
| Manufacturer | |
| RxNorm Concept Unique ID - RxCUI |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() LACRISERT 86533848 not registered Dead/Abandoned |
ATON PHARMA, INC. 2015-02-12 |
![]() LACRISERT 85448040 not registered Dead/Abandoned |
Aton Pharma, Inc. 2011-10-14 |
![]() LACRISERT 77423383 not registered Dead/Abandoned |
Aton Pharma, Inc. 2008-03-17 |
![]() LACRISERT 73233021 1156075 Live/Registered |
Merck & Co., Inc. 1979-09-27 |