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 |