Imipramine Hydrochloride
- Product NDC
- 71205-804
- 11-digit product format
- 712050804
- Labeler code
- 71205
- Product ID
- 71205-804_3f90b8dd-7234-4428-b896-943d052dd05f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Imipramine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA040903
- Marketing category
- ANDA
- Marketing start
- 2016-04-07
- Substance
- IMIPRAMINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Tricyclic Antidepressant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71205-804-30 | Imipramine Hydrochloride | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 1 |
| 71205-804-60 | Imipramine Hydrochloride | 60 in 1 BOTTLE | TABLET, FILM COATED | 60 | | 1 |
| 71205-804-90 | Imipramine Hydrochloride | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71205-804 | IMIPRAMINE HYDROCHLORIDE TABLET, FILM COATED [PROFICIENT RX LP] | 1 | Current NDC, 3 package rows | 20230613_3f90b8dd-7234-4428-b896-943d052dd05f.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 71205-804-30 | 71205080430 | 30 TABLET, FILM COATED in 1 BOTTLE (71205-804-30) | 2023-06-05 | No | No | Historical |
| 71205-804-60 | 71205080460 | 60 TABLET, FILM COATED in 1 BOTTLE (71205-804-60) | 2023-06-05 | No | No | Historical |
| 71205-804-90 | 71205080490 | 90 TABLET, FILM COATED in 1 BOTTLE (71205-804-90) | 2023-06-05 | No | No | Historical |