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Data / Drug companies / Esba Laboratories Inc.

Esba Laboratories Inc.: 5 products in the FDA NDC directory, labeler code 63135

Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).

Esba Laboratories Inc. (labeler code 63135) lists 5 products in the FDA National Drug Code Directory, covering 2 finished drugs by generic name. By type: 5 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on September 3, 2019.

The request: Watch Esba Laboratories Inc. (FDA labeler code 63135): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
63135
Products in commercial distribution
5
Packages
10
Finished drugs by generic name
2
Prescription products
0
Over the counter products
5
Flagged as original packager
5 of 5 products that carry the flag
Started marketing in the last 12 months
0
Earliest marketing start
April 20, 2003
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Over the counter monograph drugs5100%

Products by type

TypeProductsShare
Over the counter drugs5100%

Drugs it lists

Finished drugs by generic name, with how many companies list each.

DrugProductsCompanies listing it
Lidocaine 5%323
Lidocaine 4%245

Dosage forms

Dosage formProductsShare
Gel480%
Cream120%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Lubricaine63135-727GelOver the counter monograph drugsSeptember 3, 2019
Lubricaine 563135-924GelOver the counter monograph drugsMarch 20, 2019
Lipocaine 563135-811CreamOver the counter monograph drugsMarch 18, 2019
Topicaine 563135-581GelOver the counter monograph drugsApril 20, 2003
Topicaine63135-312GelOver the counter monograph drugsApril 20, 2003

CC0 1.0 public domain dedication (openFDA). Counts are products in the FDA National Drug Code Directory on November 6, 2026: 138,262 products in commercial distribution, meaning without a marketing end date in the past. A company is a labeler code; one company can hold several codes, and the directory carries no address. Inclusion in the directory is not FDA approval, and the marketing category says under which kind of application or rule a product is sold. This page uses openFDA data and is not endorsed or certified by FDA. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.