Diltiazem Hydrochloride
- Product NDC
- 63629-3564
- 11-digit product format
- 636293564
- Labeler code
- 63629
- Product ID
- 63629-3564_4f7c71ff-60c7-4694-85db-972b105fc49a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diltiazem Hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA075116
- Marketing category
- ANDA
- Marketing start
- 1999-12-28
- Marketing end
- 0000-00-00
- Substance
- DILTIAZEM HYDROCHLORIDE
- Active strength
- 240 mg/1
- Pharmacologic classes
- Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 63629-3564-1 | 2021-07-01 | C162847 | 48780-1 | 9855e2a2-4992-60a7-e053-dbdaa90a05bd | 6d7a2971-ba1d-4ec6-ab7f-9bfbcd3b7a1b |
| 63629-3564-2 | 2021-07-01 | C162847 | 48780-1 | 9855e2a2-4992-60a7-e053-dbdaa90a05bd | 6d7a2971-ba1d-4ec6-ab7f-9bfbcd3b7a1b |
| 63629-3564-1 | 2019-11-27 | C162847 | 48780-1 | 9855e2a2-4992-60a7-e053-dbdaa90a05bd | 6d7a2971-ba1d-4ec6-ab7f-9bfbcd3b7a1b |
| 63629-3564-2 | 2019-11-27 | C162847 | 48780-1 | 9855e2a2-4992-60a7-e053-dbdaa90a05bd | 6d7a2971-ba1d-4ec6-ab7f-9bfbcd3b7a1b |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 63629-3564-1 | EA - Each | 63629-3564 | d60614de-a6b4-4b1a-ad86-9f11a61b28ca | 1 | 2013-02-13 |