NA is a Oral Capsule, Delayed Release in the Human Prescription Drug category. It is labeled and distributed by Qingdao Baheal Pharmaceutical Co., Ltd.. The primary component is Duloxetine Hydrochloride.
| Product ID | 70247-013_894aaedb-aa35-23ab-e053-2a95a90a99c1 |
| NDC | 70247-013 |
| Product Type | Human Prescription Drug |
| Proprietary Name | NA |
| Generic Name | Duloxetine Delayed-release Capsules |
| Dosage Form | Capsule, Delayed Release |
| Route of Administration | ORAL |
| Marketing Start Date | 2018-05-05 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA210599 |
| Labeler Name | Qingdao BAHEAL Pharmaceutical Co., Ltd. |
| Substance Name | DULOXETINE HYDROCHLORIDE |
| Active Ingredient Strength | 30 mg/1 |
| Pharm Classes | Norepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2020-12-31 |
| Marketing Start Date | 2018-05-08 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA210599 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2018-05-08 |
| Marketing Category | ANDA |
| Application Number | ANDA210599 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2018-05-08 |
| Marketing Category | ANDA |
| Application Number | ANDA210599 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2018-05-08 |
| Ingredient | Strength |
|---|---|
| DULOXETINE HYDROCHLORIDE | 30 mg/1 |
| SPL SET ID: | e428429e-e1ea-40e1-870f-134533dc3aa1 |
| Manufacturer | |
| UNII | |
| UPC Code |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 68055-641 | NA | LIDOCAINE HYDROCHLORIDE |
| 68055-642 | NA | LIDOCAINE HYDROCHLORIDE |
| 68055-643 | NA | LIDOCAINE HYDROCHLORIDE |
| 68055-645 | NA | LIDOCAINE HYDROCHLORIDE |
| 68055-646 | NA | LIDOCAINE HYDROCHLORIDE |
| 68055-647 | NA | LIDOCAINE HYDROCHLORIDE |
| 68055-649 | NA | Lidocaine Hydrochloride |
| 70247-012 | NA | Duloxetine delayed-release capsules |
| 70247-013 | NA | Duloxetine delayed-release capsules |
| 70247-014 | NA | Duloxetine delayed-release capsules |
| 83090-001 | NA | LIDOCAINE HYDROCHLORIDE |
| 83090-002 | NA | LIDOCAINE HYDROCHLORIDE |
| 83090-003 | NA | LIDOCAINE HYDROCHLORIDE |
| 83090-004 | NA | LIDOCAINE HYDROCHLORIDE |
| 83090-005 | NA | LIDOCAINE HYDROCHLORIDE |
| 83090-006 | NA | LIDOCAINE HYDROCHLORIDE |
| 83090-007 | NA | Lidocaine Hydrochloride |