Phentermine Hydrochloride

Product NDC: 71335-1312
11-digit product format: 713351312
Labeler code: 71335
Product ID: 71335-1312_0f091a47-c71c-0d97-e063-6394a90a50bf
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Phentermine Hydrochloride
Dosage form: TABLET
Route: ORAL
Labeler: Bryant Ranch Prepack
Application: ANDA040526
Marketing category: ANDA
Marketing start: 2013-08-12
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: 2026-12-31
Current FDA listing: Yes

openFDA Listing Details

Product ID: 71335-1312_0f091a47-c71c-0d97-e063-6394a90a50bf
Product type: HUMAN PRESCRIPTION DRUG
Finished product: Yes
Brand name base: Phentermine Hydrochloride
Generic name: Phentermine Hydrochloride
Dosage form: TABLET
Route: ORAL
Marketing start: 2013-08-12
Marketing category: ANDA
Application number: ANDA040526
Pharmacologic classes: Appetite Suppression [PE]; Increased Sympathetic Activity [PE]; Sympathomimetic Amine Anorectic [EPC]
DEA schedule: CIV
Listing expiration: 2026-12-31

Ingredient	Strength
PHENTERMINE HYDROCHLORIDE	30 mg/1

UNII	Preferred term	Registry number	Matched term
0K2I505OTV	PHENTERMINE HYDROCHLORIDE	1197-21-3	PHENTERMINE HYDROCHLORIDE

Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
71335-1312-1	71335131201	30 TABLET in 1 BOTTLE (71335-1312-1)	30 tablet	2019-08-22	0000-00-00	No	No	Current

Title	Manufacturer	Effective date	Type	Version
Phentermine Hydrochloride	Bryant Ranch Prepack	2024-01-15	HUMAN PRESCRIPTION DRUG LABEL	3