Gabapentin
- Product NDC
- 70518-0483
- 11-digit product format
- 705180483
- Labeler code
- 70518
- Product ID
- 70518-0483_e1a97c9f-1269-876e-e053-2a95a90a0e22
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gabapentin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA202764
- Marketing category
- ANDA
- Marketing start
- 2017-05-05
- Marketing end
- 0000-00-00
- Substance
- GABAPENTIN
- Active strength
- 600 mg/1
- Pharmacologic classes
- Anti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-0483-0 | 70518048300 | 30 TABLET in 1 BLISTER PACK (70518-0483-0) | 30 tablet | 2017-05-05 | 0000-00-00 | No | No | Current |