Application 075606
- Type
- ANDA
- Sponsor
- PHARM ASSOC
Related Records
Application Products
| Product | Drug | Ingredient | Form | Strength | Reference drug | Reference standard |
|---|---|---|---|---|---|---|
| 001 | NORTRIPTYLINE HYDROCHLORIDE | NORTRIPTYLINE HYDROCHLORIDE | SOLUTION;ORAL | EQ 10MG BASE/5ML | No | Yes |
NDC Listings For This Application
| NDC | Name | Nonproprietary name | Labeler | Marketing category | Status |
|---|---|---|---|---|---|
| 0121-0678 | Nortriptyline Hydrochloride | Nortriptyline Hydrochloride | Pharmaceutical Associates, Inc. | ANDA | Current |
| 0121-0678 | Nortriptyline Hydrochloride | Nortriptyline Hydrochloride | Pharmaceutical Associates, Inc. | ANDA | Current |
| 0121-0678 | Nortriptyline Hydrochloride | Nortriptyline Hydrochloride | Pharmaceutical Associates, Inc. | ANDA | Current |
Documents
| Document | Submission type | Date |
|---|---|---|
| 8735 | ORIG | 2000-08-23 |