AMITRIPTYLINE HYDROCHLORIDE
- Product NDC
- 53002-4910
- 11-digit product format
- 530024910
- Labeler code
- 53002
- Product ID
- 53002-4910_97533a4a-0777-4e65-84b4-fdfbd812a47f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- AMITRIPTYLINE HYDROCHLORIDE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- RPK Pharmaceuticals, Inc.
- Application
- ANDA202446
- Marketing category
- ANDA
- Marketing start
- 2014-12-05
- Marketing end
- 0000-00-00
- Substance
- AMITRIPTYLINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Tricyclic Antidepressant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
NDC, Effective, Action table| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|
| 53002-4910-3 | 2025-01-30 | C162847 | 48780-1 | 9d75b9d0-1d2f-f424-e053-dadaa90a57ce | Amitriptyline Hydrochloride Tablets, USP |
| 53002-4910-6 | 2025-01-30 | C162847 | 48780-1 | 9d75b9d0-1d2f-f424-e053-dadaa90a57ce | Amitriptyline Hydrochloride Tablets, USP |
| 53002-4910-3 | 2023-06-07 | C162847 | 48780-1 | 9d75b9d0-1d2f-f424-e053-dadaa90a57ce | Amitriptyline Hydrochloride Tablets, USP |
| 53002-4910-6 | 2023-06-07 | C162847 | 48780-1 | 9d75b9d0-1d2f-f424-e053-dadaa90a57ce | Amitriptyline Hydrochloride Tablets, USP |
| 53002-4910-3 | 2023-01-30 | C162847 | 48780-1 | 9d75b9d0-1d2f-f424-e053-dadaa90a57ce | Amitriptyline Hydrochloride Tablets, USP |
| 53002-4910-6 | 2023-01-30 | C162847 | 48780-1 | 9d75b9d0-1d2f-f424-e053-dadaa90a57ce | Amitriptyline Hydrochloride Tablets, USP |
| 53002-4910-3 | 2020-12-17 | C162847 | 48780-1 | 9d75b9d0-1d2f-f424-e053-dadaa90a57ce | Amitriptyline Hydrochloride Tablets, USP |
| 53002-4910-6 | 2020-12-17 | C162847 | 48780-1 | 9d75b9d0-1d2f-f424-e053-dadaa90a57ce | Amitriptyline Hydrochloride Tablets, USP |
| 53002-4910-3 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-1d2f-f424-e053-dadaa90a57ce | Amitriptyline Hydrochloride Tablets, USP |
| 53002-4910-6 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-1d2f-f424-e053-dadaa90a57ce | Amitriptyline Hydrochloride Tablets, USP |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 53002-4910-3 | AMITRIPTYLINE HYDROCHLORIDE | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 5 |
| 53002-4910-6 | AMITRIPTYLINE HYDROCHLORIDE | 60 in 1 BOTTLE | TABLET, FILM COATED | 60 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53002-4910 | AMITRIPTYLINE HYDROCHLORIDE TABLET, FILM COATED [RPK PHARMACEUTICALS, INC.] | 5 | Legacy NDC, 2 package rows | 20230609_9bfd3fb2-e862-48ec-b9af-6a71eacf7b51.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 53002-4910-3 | 53002491003 | 30 TABLET, FILM COATED in 1 BOTTLE (53002-4910-3) | 2018-10-01 | 0000-00-00 | No | No | Current |
| 53002-4910-6 | 53002491006 | 60 TABLET, FILM COATED in 1 BOTTLE (53002-4910-6) | 2018-10-01 | 0000-00-00 | No | No | Current |