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Data / Drug companies / Mission Pharmacal Company

Mission Pharmacal Company: 28 products in the FDA NDC directory, labeler code 0178

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

Mission Pharmacal Company (labeler code 0178) lists 28 products in the FDA National Drug Code Directory, covering 11 finished drugs by generic name. By type: 24 prescription drugs, 4 over the counter drugs. Its main marketing category is other unapproved drugs. The newest product started marketing on October 26, 2026.

The request: Watch Mission Pharmacal Company (FDA labeler code 0178): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
0178
Products in commercial distribution
28
Packages
32
Finished drugs by generic name
11
Prescription products
24
Over the counter products
4
Flagged as original packager
25 of 25 products that carry the flag
Started marketing in the last 12 months
1
Products with a marketing end date set
1
Earliest marketing start
January 1, 1981
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Other unapproved drugs1553.6%
New drug applications (NDA)828.6%
Over the counter monograph drugs310.7%
Generic drugs (ANDA)27.1%

Products by type

TypeProductsShare
Prescription drugs2485.7%
Over the counter drugs414.3%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Cream621.4%
Liquid310.7%
Tablet, film coated310.7%
Emulsion27.1%
Tablet, delayed release27.1%
Tablet27.1%
Solution27.1%
Tablet, extended release27.1%
Tablet, coated13.6%
Kit13.6%
Shampoo13.6%
Ointment13.6%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Theragesic0178-0320CreamOver the counter monograph drugsOctober 26, 2026
Uribel tabs0178-0745Tablet, coatedOther unapproved drugsNovember 7, 2023
Thiola EC0178-0902Tablet, delayed releaseNew drug applications (NDA)June 28, 2019
Thiola EC0178-0901Tablet, delayed releaseNew drug applications (NDA)June 28, 2019
Potassium iodide0178-0314SolutionGeneric drugs (ANDA)May 15, 2016
CitraNatal Assure0178-0891KitOther unapproved drugsApril 30, 2014
CitraNatal 90 DHA0178-0821TabletOther unapproved drugsApril 11, 2014
Texacort0178-0455SolutionGeneric drugs (ANDA)December 15, 2011
Ovace Plus0178-0620LotionOther unapproved drugsSeptember 15, 2011
Ovace0178-0499LiquidOther unapproved drugsSeptember 15, 2011
OvacePlus Plus0178-0495CreamOther unapproved drugsSeptember 15, 2011
OVACE Plus0178-0490LiquidOther unapproved drugsSeptember 15, 2011
OVACE Plus0178-0485ShampooOther unapproved drugsSeptember 15, 2011
Avar0178-0480EmulsionOther unapproved drugsSeptember 15, 2011
Avar ls0178-0475EmulsionOther unapproved drugsSeptember 15, 2011
Avar-e0178-0470CreamOther unapproved drugsSeptember 15, 2011
Avar-e LS0178-0465CreamOther unapproved drugsSeptember 15, 2011
Avar-e Green0178-0460CreamOther unapproved drugsSeptember 15, 2011
Ovace plus0178-0630LiquidOther unapproved drugsSeptember 7, 2011
Dr smiths diaper0178-0330OintmentOver the counter monograph drugsMarch 1, 2010
Ferralet 900178-0089Tablet, film coatedOther unapproved drugsFebruary 4, 2010
Urocit-k0178-0615Tablet, extended releaseNew drug applications (NDA)January 27, 2010
Tindamax0178-8500Tablet, film coatedNew drug applications (NDA)May 17, 2004
Tindamax0178-8250Tablet, film coatedNew drug applications (NDA)May 17, 2004
Urocit-k0178-0610Tablet, extended releaseNew drug applications (NDA)September 1, 1992

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.