Imipramine Hydrochloride
- Product NDC
- 70518-3526
- 11-digit product format
- 705183526
- Labeler code
- 70518
- Product ID
- 70518-3526_4f56ae1d-2dd1-efad-e063-6394a90ae915
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Imipramine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA040751
- Marketing category
- ANDA
- Marketing start
- 2020-09-19
- Substance
- IMIPRAMINE HYDROCHLORIDE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Tricyclic Antidepressant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Imipramine Hydrochloride
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| IMIPRAMINE HYDROCHLORIDE | 25 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | BKE5Q1J60U |
| Rxcui | 835564 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70518-3526-0 | Imipramine Hydrochloride | 30 in 1 BLISTER PACK | TABLET | 30 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-3526 | IMIPRAMINE HYDROCHLORIDE TABLET [REMEDYREPACK INC.] | 2 | Current NDC, Legacy NDC, 1 package rows | 20240116_02c19a0a-3d9d-4881-ad14-1687aafd87b5.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-3526-0 | 70518352600 | 30 TABLET in 1 BLISTER PACK (70518-3526-0) | 30 tablet | 2020-09-19 | 0000-00-00 | No | No | Current |