Data / Drug companies / Qingdao Baheal Pharmaceutical Co., Ltd.
Qingdao Baheal Pharmaceutical Co., Ltd.: 9 products in the FDA NDC directory, labeler code 70247
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Qingdao Baheal Pharmaceutical Co., Ltd. (labeler code 70247) lists 9 products in the FDA National Drug Code Directory, covering 3 finished drugs by generic name. By type: 9 prescription drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on December 27, 2018.
The request: Watch Qingdao Baheal Pharmaceutical Co., Ltd. (FDA labeler code 70247): each new product listing and each discontinued product. $10 of work on sign-up, no card.
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- Labeler code
- 70247
- Products in commercial distribution
- 9
- Packages
- 15
- Finished drugs by generic name
- 3
- Prescription products
- 9
- Over the counter products
- 0
- Flagged as original packager
- 9 of 9 products that carry the flag
- Started marketing in the last 12 months
- 0
- Earliest marketing start
- October 10, 2016
- openFDA record search
- api.fda.gov
Products by marketing category
Share of the company's products in commercial distribution.
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 9 | 100% |
Products by type
| Type | Products | Share |
|---|---|---|
| Prescription drugs | 9 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Celecoxib | 4 | 63 |
| Duloxetine | 3 | 36 |
| Metformin hydrochloride extended-release tablets | 2 | 3 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Capsule | 4 | 44.4% |
| Capsule, delayed release | 3 | 33.3% |
| Tablet, film coated, extended release | 2 | 22.2% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
| Class | Products |
|---|---|
| Nonsteroidal Anti-inflammatory Drug | 4 |
| Serotonin and Norepinephrine Reuptake Inhibitor | 3 |
| Biguanide | 2 |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Metformin Hydrochloride | 70247-019 | Tablet, film coated, extended release | Generic drugs (ANDA) | December 27, 2018 |
| Metformin Hydrochloride | 70247-018 | Tablet, film coated, extended release | Generic drugs (ANDA) | December 27, 2018 |
| Duloxetine | 70247-014 | Capsule, delayed release | Generic drugs (ANDA) | May 5, 2018 |
| Duloxetine | 70247-013 | Capsule, delayed release | Generic drugs (ANDA) | May 5, 2018 |
| Duloxetine | 70247-012 | Capsule, delayed release | Generic drugs (ANDA) | May 5, 2018 |
| Celecoxib | 70247-009 | Capsule | Generic drugs (ANDA) | October 10, 2016 |
| Celecoxib | 70247-008 | Capsule | Generic drugs (ANDA) | October 10, 2016 |
| Celecoxib | 70247-007 | Capsule | Generic drugs (ANDA) | October 10, 2016 |
| Celecoxib | 70247-006 | Capsule | Generic drugs (ANDA) | October 10, 2016 |
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.