Phentermine Hydrochloride
- Product NDC
- 49999-517
- 11-digit product format
- 499990517
- Labeler code
- 49999
- Product ID
- 49999-517_50c79990-4609-4b6b-8b74-ccc0231a63f8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phentermine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products
- Application
- ANDA040876
- Marketing category
- ANDA
- Marketing start
- 2012-08-15
- Marketing end
- 0000-00-00
- Substance
- PHENTERMINE HYDROCHLORIDE
- Active strength
- 38 mg/1
- Pharmacologic classes
- Appetite Suppression [PE],Increased Sympathetic Activity [PE],Sympathomimetic Amine Anorectic [EPC]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 49999-517-07 | EA - Each | 49999-517 | b2bacb9c-7158-43f8-b474-4ca9f1da1b38 | 1 | 2015-10-02 |
| 49999-517-14 | EA - Each | 49999-517 | d5ae3562-da43-4a6c-946b-9e159a5ac517 | 1 | 2015-10-02 |
| 49999-517-15 | EA - Each | 49999-517 | 66270a7c-e046-479c-b487-1dd3d3865dfb | 1 | 2014-08-01 |
| 49999-517-28 | EA - Each | 49999-517 | 2f03aa48-336e-46e5-aaf9-4d6ed9c6e41a | 1 | 2015-10-02 |
| 49999-517-30 | EA - Each | 49999-517 | a0385422-d2f9-410c-bf76-46413fd2ec02 | 1 | 2014-08-01 |
| 49999-517-45 | EA - Each | 49999-517 | 0bcf77c0-5aad-4f04-9cfd-38867933a85a | 1 | 2014-08-01 |
| 49999-517-60 | EA - Each | 49999-517 | 4ec18358-077e-4fd9-8f1e-2217ca51fb2b | 1 | 2014-08-01 |