Gabapentin 300 mg capsule
Public data on gabapentin from CMS and FDA: what pharmacies have paid for it, how many generic applications FDA has approved, and whether it appears in FDA's shortage or recall records.
NADAC per unit, monthly
GABAPENTIN 300 MG CAPSULEShow as table
| Month | NADAC per unit ($) |
|---|---|
| 2013-11 | 0.05637 |
| 2014-02 | 0.06302 |
| 2014-05 | 0.05636 |
| 2014-08 | 0.05217 |
| 2014-11 | 0.04671 |
| 2015-02 | 0.04924 |
| 2015-05 | 0.04978 |
| 2015-08 | 0.04692 |
| 2015-11 | 0.04470 |
| 2016-02 | 0.04461 |
| 2016-05 | 0.04372 |
| 2016-08 | 0.04659 |
| 2016-11 | 0.04073 |
| 2017-02 | 0.04131 |
| 2017-05 | 0.04049 |
| 2017-08 | 0.04212 |
| 2017-11 | 0.04034 |
| 2018-02 | 0.04325 |
| 2018-05 | 0.04382 |
| 2018-08 | 0.04719 |
| 2018-11 | 0.05717 |
| 2019-02 | 0.05351 |
| 2019-05 | 0.05115 |
| 2019-08 | 0.05394 |
| 2019-11 | 0.05572 |
| 2020-02 | 0.05454 |
| 2020-05 | 0.05791 |
| 2020-08 | 0.05498 |
| 2020-11 | 0.05120 |
| 2021-02 | 0.04967 |
| 2021-05 | 0.04988 |
| 2021-08 | 0.05091 |
| 2021-11 | 0.05098 |
| 2022-02 | 0.05194 |
| 2022-05 | 0.04676 |
| 2022-08 | 0.04771 |
| 2022-11 | 0.04479 |
| 2023-02 | 0.04392 |
| 2023-05 | 0.04254 |
| 2023-08 | 0.04113 |
| 2023-11 | 0.04095 |
| 2024-02 | 0.04069 |
| 2024-05 | 0.03788 |
| 2024-08 | 0.03808 |
| 2024-11 | 0.03454 |
| 2025-02 | 0.03603 |
| 2025-05 | 0.03488 |
| 2025-08 | 0.03596 |
| 2025-11 | 0.03386 |
| 2026-02 | 0.03378 |
| 2026-05 | 0.03246 |
| 2026-08 | 0.03046 |
| 2026-11 | 0.03283 |
Source: CMS NADAC weekly files, generic rows, monthly median of weekly averages · data as of 2026-11. Figures can change and may contain errors in the source data. Check the original source before relying on them.
Recall records mentioning gabapentin
openFDA enforcement records, by year reported.
| 2025 | 7 |
| 2024 | 1 |
| 2023 | 2 |
| 2021 | 1 |
| 2020 | 2 |
| 2019 | 2 |
| 2018 | 3 |
| 2015 | 5 |
| 2014 | 1 |
| 2013 | 1 |
25 records since 2012. A record is one product or lot, not one recall event. Combination products that contain gabapentin are included.
What these numbers mean
NADAC is what retail pharmacies pay on average to buy the drug, published by CMS. It does not include rebates and is not what you pay at the counter. ANDA counts include all strengths and forms and applications whose products are now discontinued.
Most recent recall records
Not health advice. GxRadar is for general information only. Nothing here is medical, pharmacy, legal or financial advice. Do not start, stop or change any medicine based on this site. Talk to your pharmacist or prescriber about your own situation.
Articles that mention gabapentin
13 GxRadar articles cite or discuss this drug.
What pharmacies paid for gabapentin, 2013 to 2026
The pharmacy cost of a generic 300 mg gabapentin capsule fell from 5.6 cents in 2013 to a series low of 3.0 cents in September 2026, with a sharp rise in between. The NADAC record and the FDA approvals behind it.
What pharmacies pay for a month of common generics
Thirty tablets of each of the 10 most-used generics we track cost pharmacies $35.70 in January 2014 and $8.80 in October 2026. That is acquisition cost, and the rest of the price sits on top of it.
Boxed warnings, FDA's most prominent label warning, explained
What 21 CFR 201.57 requires of a boxed warning, how many prescription labels carry one (about a third, by two counts 14 years apart), and why a generic's box matches the brand's.
Generics fill 84.5% of Medicare Part D claims and account for 11.6% of the cost
CMS grand totals for 2013 to 2024 show the generic share of Part D claims rising and the generic share of cost falling, plus a 2024 drop in generic spending that matches a pricing rule change.
Pediatric exclusivity and the six months it adds before generics
A brand company that studies its drug in children at FDA's written request can win six more months of protection from generics. How the 1997 incentive works, what it attaches to, and what FDA's own lists show.
Unit-dose and blister packaging, from hospital carts to dose packs
How unit-dose systems spread through US hospitals, what FDA requires on unit-dose and blister labels, the six-month dating rule for repackaged doses, and how blister packs fail.