GABAPENTIN
- Product NDC
- 71205-619
- 11-digit product format
- 712050619
- Labeler code
- 71205
- Product ID
- 71205-619_185f264e-db32-41cd-b90d-519717b97850
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- GABAPENTIN
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA075360
- Marketing category
- ANDA
- Marketing start
- 2020-09-07
- Substance
- GABAPENTIN
- Active strength
- 400 mg/1
- Pharmacologic classes
- Anti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 6CW7F3G59X | GABAPENTIN | 60142-96-3 | GABAPENTIN |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71205-619-30 | 71205061930 | 30 CAPSULE in 1 BOTTLE (71205-619-30) | 30 capsule | 2021-11-02 | No | No | Historical |
| 71205-619-60 | 71205061960 | 60 CAPSULE in 1 BOTTLE (71205-619-60) | 60 capsule | 2021-11-02 | No | No | Historical |
| 71205-619-72 | 71205061972 | 120 CAPSULE in 1 BOTTLE (71205-619-72) | 120 capsule | 2021-11-02 | No | No | Historical |
| 71205-619-90 | 71205061990 | 90 CAPSULE in 1 BOTTLE (71205-619-90) | 90 capsule | 2021-11-02 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| GABAPENTIN | Proficient Rx LP | 2021-11-01 | HUMAN PRESCRIPTION DRUG LABEL | 1 |