Phentermine Hydrochloride
- Product NDC
- 63629-1045
- 11-digit product format
- 636291045
- Labeler code
- 63629
- Product ID
- 63629-1045_17745e52-1a98-4002-939a-2880f92007d4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phentermine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA200272
- Marketing category
- ANDA
- Marketing start
- 2011-03-08
- 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 |
|---|
| 63629-1045 | PHENTERMINE HYDROCHLORIDE TABLET [BRYANT RANCH PREPACK] | 6 | Legacy NDC | 20240607_a458bc67-ff80-4cb8-b718-c01e48849816.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-1045-1 | 63629104501 | 1000 TABLET in 1 BOTTLE (63629-1045-1) | 1000 tablet | 2019-07-01 | 0000-00-00 | No | No | Current |