Propranolol Hydrochloride
- Product NDC
- 63629-4610
- 11-digit product format
- 636294610
- Labeler code
- 63629
- Product ID
- 63629-4610_aad51968-d672-4ea6-bc42-bdbbe8319e3c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Propranolol Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA078955
- Marketing category
- ANDA
- Marketing start
- 2008-10-13
- Marketing end
- 0000-00-00
- Substance
- PROPRANOLOL HYDROCHLORIDE
- Active strength
- 40 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA],beta-Adrenergic 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 |
|---|---|---|---|---|---|
| 63629-4610-1 | 2019-12-11 | C162847 | 48780-1 | 9855d018-dc1f-cd31-e053-dbdaa90ab51a | 2b26c3aa-2762-471c-9140-c5084d695da4 |
| 63629-4610-2 | 2019-12-11 | C162847 | 48780-1 | 9855d018-dc1f-cd31-e053-dbdaa90ab51a | 2b26c3aa-2762-471c-9140-c5084d695da4 |
| 63629-4610-3 | 2019-12-11 | C162847 | 48780-1 | 9855d018-dc1f-cd31-e053-dbdaa90ab51a | 2b26c3aa-2762-471c-9140-c5084d695da4 |
| 63629-4610-4 | 2019-12-11 | C162847 | 48780-1 | 9855d018-dc1f-cd31-e053-dbdaa90ab51a | 2b26c3aa-2762-471c-9140-c5084d695da4 |
| 63629-4610-1 | 2019-11-27 | C162847 | 48780-1 | 9855d018-dc1f-cd31-e053-dbdaa90ab51a | 2b26c3aa-2762-471c-9140-c5084d695da4 |
| 63629-4610-2 | 2019-11-27 | C162847 | 48780-1 | 9855d018-dc1f-cd31-e053-dbdaa90ab51a | 2b26c3aa-2762-471c-9140-c5084d695da4 |
| 63629-4610-3 | 2019-11-27 | C162847 | 48780-1 | 9855d018-dc1f-cd31-e053-dbdaa90ab51a | 2b26c3aa-2762-471c-9140-c5084d695da4 |
| 63629-4610-4 | 2019-11-27 | C162847 | 48780-1 | 9855d018-dc1f-cd31-e053-dbdaa90ab51a | 2b26c3aa-2762-471c-9140-c5084d695da4 |