Tamsulosin Hydrochloride
- Product NDC
- 63739-811
- 11-digit product format
- 637390811
- Labeler code
- 63739
- Product ID
- 63739-811_bdb538ba-c887-4241-ac4e-adc6ecd21c83
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tamsulosin hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- McKesson Corporation dba SKY Packaging
- Application
- ANDA078801
- Marketing category
- ANDA
- Marketing start
- 2010-04-27
- Marketing end
- 0000-00-00
- Substance
- TAMSULOSIN HYDROCHLORIDE
- Active strength
- 0 mg/1
- Pharmacologic classes
- Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 63739-811-41 | 2020-07-22 | C162847 | 48780-1 | ab0e2407-3587-f274-e053-dbdaa90a6471 | acbaeb6c-1198-4d11-8016-e8b6dcbbc5d9 |
| 63739-811-43 | 2020-07-22 | C162847 | 48780-1 | ab0e2407-3587-f274-e053-dbdaa90a6471 | acbaeb6c-1198-4d11-8016-e8b6dcbbc5d9 |
| 63739-811-45 | 2020-07-22 | C162847 | 48780-1 | ab0e2407-3587-f274-e053-dbdaa90a6471 | acbaeb6c-1198-4d11-8016-e8b6dcbbc5d9 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 63739-811-41 | EA - Each | 63739-811 | bf7a706b-5090-4086-a491-c78e8b57953b | 1 | 2013-03-03 |
| 63739-811-43 | EA - Each | 63739-811 | 73d2f8a5-ce40-4015-9f00-2dd1ddf7a5a2 | 1 | 2013-11-04 |
| 63739-811-45 | EA - Each | 63739-811 | c58a4d87-4c5b-489a-a527-b68607d4785a | 1 | 2013-11-04 |