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Data / Drug companies / Pacific Pharma, Inc.

Pacific Pharma, Inc.: 6 products in the FDA NDC directory, labeler code 60758

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

Pacific Pharma, Inc. (labeler code 60758) lists 6 products in the FDA National Drug Code Directory, covering 5 finished drugs by generic name. By type: 6 prescription drugs. Its main marketing category is authorized generics (NDA). The newest product started marketing on October 18, 2017.

The request: Watch Pacific Pharma, Inc. (FDA labeler code 60758): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
60758
Products in commercial distribution
6
Packages
13
Finished drugs by generic name
5
Prescription products
6
Over the counter products
0
Flagged as original packager
6 of 6 products that carry the flag
Started marketing in the last 12 months
0
Earliest marketing start
May 20, 1997
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Authorized generics (NDA)466.7%
Generic drugs (ANDA)233.3%

Products by type

TypeProductsShare
Prescription drugs6100%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Solution/ drops466.7%
Gel116.7%
Suspension/ drops116.7%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Dapsone60758-670GelAuthorized generics (NDA)October 18, 2017
Ketorolac tromethamine60758-773Solution/ dropsAuthorized generics (NDA)November 21, 2013
Fluorometholone60758-880Solution/ dropsAuthorized generics (NDA)October 31, 1997
Prednisolone acetate60758-119Suspension/ dropsAuthorized generics (NDA)August 19, 1997
Timolol maleate60758-802Solution/ dropsGeneric drugs (ANDA)May 20, 1997
Timolol maleate60758-801Solution/ dropsGeneric drugs (ANDA)May 20, 1997

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.