Data / Drug companies / Green Pharmaceuticals Inc
Green Pharmaceuticals Inc: 6 products in the FDA NDC directory, labeler code 61152
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Green Pharmaceuticals Inc (labeler code 61152) lists 6 products in the FDA National Drug Code Directory. By type: 6 over the counter drugs. Its main marketing category is unapproved homeopathic products. The newest product started marketing on April 1, 2026.
The request: Watch Green Pharmaceuticals Inc (FDA labeler code 61152): each new product listing and each discontinued product. $10 of work on sign-up, no card.
SpecStream is the live web data engine for teams and agents. It reads the National Drug Code Directory that FDA publishes, and this page is that reading. Ask for the companies that make a drug, a class or a dosage form, with their headquarters, website and size added from the web, and new listings and discontinued products arrive in your sheet, CRM, Slack or agent as FDA posts them.
- Labeler code
- 61152
- Products in commercial distribution
- 6
- Packages
- 6
- Finished drugs by generic name
- 0
- Prescription products
- 0
- Over the counter products
- 6
- Flagged as original packager
- 5 of 5 products that carry the flag
- Started marketing in the last 12 months
- 1
- Earliest marketing start
- August 1, 2012
- openFDA record search
- api.fda.gov
Products by marketing category
Share of the company's products in commercial distribution.
| Marketing category | Products | Share |
|---|---|---|
| Unapproved homeopathic products | 6 | 100% |
Products by type
| Type | Products | Share |
|---|---|---|
| Over the counter drugs | 6 | 100% |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Spray | 4 | 66.7% |
| Tablet, chewable | 1 | 16.7% |
| Kit | 1 | 16.7% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
| Class | Products |
|---|---|
| Non-Standardized Plant Allergenic Extract | 5 |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Snore Stop OralSpray | 61152-601 | Spray | Unapproved homeopathic products | April 1, 2026 |
| Snorestop | 61152-600 | Spray | Unapproved homeopathic products | June 19, 2025 |
| SnoreStop Extinguisher 120 | 61152-400 | Spray | Unapproved homeopathic products | August 1, 2022 |
| SnoreStop Double Action | 61152-200 | Kit | Unapproved homeopathic products | August 1, 2022 |
| Snore Stop Extinguisher Throat | 61152-196 | Spray | Unapproved homeopathic products | December 28, 2012 |
| SnoreStop Chewable Fast tabs 60 | 61152-100 | Tablet, chewable | Unapproved homeopathic products | August 1, 2012 |
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.