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 |