Phentermine Hydrochloride
- Product NDC
- 43063-332
- 11-digit product format
- 430630332
- Labeler code
- 43063
- Product ID
- 43063-332_5bb0b7c6-12be-0ad5-e053-2a91aa0a5006
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phentermine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA040526
- Marketing category
- ANDA
- Marketing start
- 2003-10-23
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 43063-332-07 | EA - Each | 43063-332 | e5020265-c88b-4f0e-86b1-d6047bb6d6eb | 1 | 2013-02-13 |
| 43063-332-14 | EA - Each | 43063-332 | 93bb8a1f-6cf1-4428-8efb-4862ccc5c987 | 1 | 2013-02-13 |
| 43063-332-15 | EA - Each | 43063-332 | e0d98673-78f2-4a23-86c5-dd9577e1c484 | 1 | 2012-07-24 |
| 43063-332-21 | EA - Each | 43063-332 | 81c0bee1-5768-4bb9-b13a-da1b9ff02527 | 1 | 2012-07-24 |
| 43063-332-28 | EA - Each | 43063-332 | 18d9b68f-0418-4967-8bd8-348297dc131d | 1 | 2013-02-13 |
| 43063-332-30 | EA - Each | 43063-332 | c0c04905-389c-4375-b43b-0a2544618da8 | 1 | 2013-02-13 |
| 43063-332-42 | EA - Each | 43063-332 | e5ca3488-04e1-49a1-8c60-d37788e28bb8 | 1 | 2012-07-24 |
| 43063-332-45 | EA - Each | 43063-332 | 4e6d56c1-32cb-41c9-ab24-5ca26bb42bf6 | 1 | 2013-02-13 |
| 43063-332-60 | EA - Each | 43063-332 | 17004756-8134-4e41-8dad-fb06eb89824d | 1 | 2013-02-13 |
| 43063-332-90 | EA - Each | 43063-332 | 0b58b2bd-9b6b-49b3-9144-8515aa7a16e6 | 1 | 2014-09-03 |
| 43063-332-93 | EA - Each | 43063-332 | 30faca4d-a7c1-49bb-8df0-a42afb8b44bd | 1 | 2014-09-03 |