Lacrisert
- Product NDC
- 24208-800
- 11-digit product format
- 242080800
- Labeler code
- 24208
- Product ID
- 24208-800_bf5e5593-8a62-4993-8895-b2a3223512d1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- hydroxypropyl cellulose
- Dosage form
- INSERT
- Route
- OPHTHALMIC
- Labeler
- Bausch & Lomb Incorporated
- Application
- NDA018771
- Marketing category
- NDA
- Marketing start
- 1981-06-01
- Marketing end
- 0000-00-00
- Substance
- HYDROXYPROPYL CELLULOSE (1600000 WAMW)
- Active strength
- 5 mg/1
- Pharmacologic classes
- Demulcent [EPC],Demulcent Activity [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 24208-800 | LACRISERT (HYDROXYPROPYL CELLULOSE) INSERT [BAUSCH & LOMB INCORPORATED] | 8 | Legacy NDC | 20240726_cc7a6a52-0b77-4df7-8403-dd21c1334f6c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 24208-800-10 | 24208080010 | 10 BLISTER PACK in 1 CARTON (24208-800-10) > 1 INSERT in 1 BLISTER PACK | 10 blister pack | 1981-06-01 | 0000-00-00 | No | No | Current |
| 24208-800-60 | 24208080060 | 60 BLISTER PACK in 1 CARTON (24208-800-60) > 1 INSERT in 1 BLISTER PACK | 60 blister pack | 1981-06-01 | 0000-00-00 | No | No | Current |