Phentermine Hydrochloride
- Product NDC
- 76420-057
- 11-digit product format
- 764200057
- Labeler code
- 76420
- Product ID
- 76420-057_ead26ce5-33db-58dc-e053-2995a90a06c6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phentermine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Asclemed USA, Inc.
- Application
- ANDA040555
- Marketing category
- ANDA
- Marketing start
- 2005-04-15
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 76420-057 | PHENTERMINE HYDROCHLORIDE TABLET [ASCLEMED USA, INC.] | 2 | Legacy NDC | 20221013_dc0bcab7-7e9a-4aef-bc4c-f44421e2202a.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 76420-057-30 | 76420005730 | 30 TABLET in 1 BOTTLE (76420-057-30) | 30 tablet | 2020-02-12 | 0000-00-00 | No | No | Current |