Clonidine Hydrochloride
- Product NDC
- 51079-300
- 11-digit product format
- 510790300
- Labeler code
- 51079
- Product ID
- 51079-300_9a250335-e14c-c9ad-e053-2a95a90a08c8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- clonidine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Mylan Institutional Inc.
- Application
- ANDA070317
- Marketing category
- ANDA
- Marketing start
- 1995-06-12
- Marketing end
- 2020-09-30
- Substance
- CLONIDINE HYDROCHLORIDE
- Active strength
- 0 mg/1
- Pharmacologic classes
- Adrenergic alpha2-Agonists [MoA],Central alpha-2 Adrenergic Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 51079-300-01 | EA - Each | 51079-300 | eeb604ca-9901-482b-9e2d-6b075da8a7f8 | 1 | 2012-07-24 |
| 51079-300-17 | EA - Each | 51079-300 | 42080ccd-f2b7-4aef-b05e-5bcb5aec0b21 | 1 | 2012-07-24 |
| 51079-300-19 | EA - Each | 51079-300 | cfccfe3c-f1e8-43bc-8398-3332f2878f5e | 1 | 2012-07-24 |
| 51079-300-20 | EA - Each | 51079-300 | aa696e05-b94c-40db-bb3e-b2ab4beb99bc | 1 | 2012-07-24 |
| 51079-300-30 | EA - Each | 51079-300 | 0b4f8f86-bdb2-4b88-ac22-36c465718b87 | 1 | 2012-07-24 |
| 51079-300-56 | EA - Each | 51079-300 | 0ec245e9-2985-4d23-a687-a480987b8419 | 1 | 2012-07-24 |
| 51079-300-66 | EA - Each | 51079-300 | 63a58cfb-e617-458d-a657-9b3c6812834e | 1 | 2012-07-24 |