Tofranil
- Product NDC
- 69874-992
- 11-digit product format
- 698740992
- Labeler code
- 69874
- Product ID
- 69874-992_b16cb744-b0d8-4f1a-a32e-43b20fe074be
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Imipramine hydrochloride
- Dosage form
- TABLET, SUGAR COATED
- Route
- ORAL
- Labeler
- Thompson Medical Solutions LLC
- Application
- ANDA087844
- Marketing category
- ANDA
- Marketing start
- 2016-12-23
- Marketing end
- 0000-00-00
- Substance
- IMIPRAMINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Tricyclic Antidepressant [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 69874-992-01 | Tofranil | 100 in 1 BOTTLE | TABLET, SUGAR COATED | 100 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69874-992 | TOFRANIL (IMIPRAMINE HYDROCHLORIDE) TABLET, SUGAR COATED [THOMPSON MEDICAL SOLUTIONS LLC] | 1 | Legacy NDC, 1 package rows | 20161230_e6aba45c-9e3c-4d14-82ce-fda3ba771fe1.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 69874-992-01 | 69874099201 | 100 in 1 BOTTLE | Historical |