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Data / Drug companies / Larken Laboratories, Inc.

Larken Laboratories, Inc.: 13 products in the FDA NDC directory, labeler code 68047

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

Larken Laboratories, Inc. (labeler code 68047) lists 13 products in the FDA National Drug Code Directory, covering 5 finished drugs by generic name. By type: 8 prescription drugs, 5 over the counter drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on July 30, 2026.

The request: Watch Larken Laboratories, Inc. (FDA labeler code 68047): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
68047
Products in commercial distribution
13
Packages
19
Finished drugs by generic name
5
Prescription products
8
Over the counter products
5
Controlled substance products
Schedule III 3
Flagged as original packager
8 of 8 products that carry the flag
Started marketing in the last 12 months
1
Products with a marketing end date set
1
Earliest marketing start
September 15, 2003
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Generic drugs (ANDA)646.2%
Over the counter monograph drugs538.5%
Other unapproved drugs215.4%

Products by type

TypeProductsShare
Prescription drugs861.5%
Over the counter drugs538.5%

Drugs it lists

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

DrugProductsCompanies listing it
Butalbital and acetaminophen39
Chlorpheniramine maleate / pseudoephedrine hcl21
Hyoscyamine sulfate224
Dexamethasone 1.5 mg22
Doxycycline hyclate161

Dosage forms

Dosage formProductsShare
Tablet753.8%
Liquid538.5%
Tablet, orally disintegrating17.7%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
LoHist-D68047-159LiquidOver the counter monograph drugsJuly 30, 2026
Dexamethasone 1.5 mg68047-702TabletGeneric drugs (ANDA)September 1, 2017
Dexamethasone 1.5 mg68047-702TabletGeneric drugs (ANDA)September 1, 2017
Butalbital and Acetaminophen68047-753TabletGeneric drugs (ANDA)December 4, 2015
Allzital68047-752TabletGeneric drugs (ANDA)December 4, 2015
Butalbital And Acetaminophen68047-721TabletGeneric drugs (ANDA)December 4, 2015
LoHist DM68047-129LiquidOver the counter monograph drugsJune 1, 2012
EndaCof DM68047-143LiquidOver the counter monograph drugsMarch 30, 2012
Oscimin68047-253Tablet, orally disintegratingOther unapproved drugsAugust 3, 2011
Oscimin68047-252TabletOther unapproved drugsAugust 3, 2011
NoHist DM68047-186LiquidOver the counter monograph drugsJanuary 6, 2011
Doxycycline Hyclate68047-714TabletGeneric drugs (ANDA)November 15, 2010
LoHist D68047-120LiquidOver the counter monograph drugsSeptember 15, 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.