Phentermine Hydrochloride
- Product NDC
- 31722-359
- 11-digit product format
- 317220359
- Labeler code
- 31722
- Product ID
- 31722-359_f8c27541-e9d7-4045-82f7-db4729db7273
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phentermine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Camber Pharmaceuticals, Inc.
- Application
- ANDA202942
- Marketing category
- ANDA
- Marketing start
- 2014-04-02
- 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
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 31722-359 | PHENTERMINE HYDROCHLORIDE TABLET [CAMBER PHARMACEUTICALS, INC.] | 1 | Legacy NDC | 20140403_a1db6d2d-d336-4534-bcd3-38ed29e46ff9.zip |