Phentermine Hydrochloride
- Product NDC
- 17224-650
- 11-digit product format
- 172240650
- Labeler code
- 17224
- Product ID
- 17224-650_9214ab52-2148-4790-9681-4fa3508bb26d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phentermine Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- CALVIN, SCOTT AND COMPANY, INCORPORATED
- Application
- ANDA040886
- Marketing category
- ANDA
- Marketing start
- 2012-08-07
- Marketing end
- 0000-00-00
- Substance
- PHENTERMINE HYDROCHLORIDE
- Active strength
- 30 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 Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 17224-650-28 | Phentermine Hydrochloride | 28 in 1 BOTTLE | CAPSULE | 28 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 17224-650 | PHENTERMINE HYDROCHLORIDE CAPSULE [CALVIN, SCOTT AND COMPANY, INCORPORATED] | 2 | Legacy NDC, 1 package rows | 20191120_0ec83de8-0ee1-47e2-bfda-5bc724fd2443.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 17224-650-28 | 17224065028 | 28 in 1 BOTTLE | Historical |